Other mutations in this stock |
Total: 418 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700086D15Rik |
A |
G |
11: 65,044,114 (GRCm39) |
W27R |
unknown |
Het |
1700086D15Rik |
A |
G |
11: 65,044,080 (GRCm39) |
F38S |
unknown |
Het |
1700086D15Rik |
A |
C |
11: 65,043,809 (GRCm39) |
V84G |
unknown |
Het |
1700086D15Rik |
T |
A |
11: 65,043,794 (GRCm39) |
Q89L |
unknown |
Het |
1700086D15Rik |
A |
G |
11: 65,044,128 (GRCm39) |
L22P |
unknown |
Het |
1810065E05Rik |
C |
T |
11: 58,313,027 (GRCm39) |
L27F |
probably benign |
Het |
1810065E05Rik |
C |
T |
11: 58,316,625 (GRCm39) |
L202F |
probably benign |
Het |
1810065E05Rik |
C |
T |
11: 58,313,060 (GRCm39) |
L38F |
possibly damaging |
Het |
2810021J22Rik |
C |
T |
11: 58,771,361 (GRCm39) |
A281V |
probably benign |
Het |
4930438A08Rik |
A |
G |
11: 58,184,844 (GRCm39) |
T521A |
unknown |
Het |
4933427D14Rik |
G |
A |
11: 72,067,535 (GRCm39) |
T585I |
possibly damaging |
Het |
4933427D14Rik |
T |
G |
11: 72,089,750 (GRCm39) |
S45R |
probably damaging |
Het |
4933427D14Rik |
C |
A |
11: 72,089,360 (GRCm39) |
A175S |
probably benign |
Het |
4933427D14Rik |
G |
A |
11: 72,089,308 (GRCm39) |
P192L |
probably benign |
Het |
4933427D14Rik |
T |
TCCCCAGC |
11: 72,086,590 (GRCm39) |
|
probably null |
Het |
4933427D14Rik |
T |
G |
11: 72,086,580 (GRCm39) |
K277T |
probably damaging |
Het |
4933427D14Rik |
A |
G |
11: 72,086,569 (GRCm39) |
C281R |
possibly damaging |
Het |
4933427D14Rik |
AAAAGTAA |
AAA |
11: 72,086,538 (GRCm39) |
|
probably null |
Het |
4933427D14Rik |
GGAAAAG |
GG |
11: 72,086,536 (GRCm39) |
|
probably null |
Het |
4933427D14Rik |
G |
T |
11: 72,080,442 (GRCm39) |
P408H |
probably damaging |
Het |
Adgra3 |
G |
A |
5: 50,136,421 (GRCm39) |
A688V |
probably damaging |
Het |
Adh1 |
T |
C |
3: 137,992,544 (GRCm39) |
I220T |
probably damaging |
Het |
Adh4 |
T |
C |
3: 138,125,091 (GRCm39) |
|
probably null |
Het |
Akap10 |
T |
A |
11: 61,806,096 (GRCm39) |
S211C |
probably benign |
Het |
Alg10b |
C |
A |
15: 90,112,397 (GRCm39) |
L414I |
possibly damaging |
Het |
Alox8 |
A |
G |
11: 69,088,322 (GRCm39) |
V76A |
probably benign |
Het |
Alox8 |
C |
T |
11: 69,076,873 (GRCm39) |
R536Q |
probably benign |
Het |
Aloxe3 |
A |
G |
11: 69,019,501 (GRCm39) |
Q138R |
probably benign |
Het |
Aloxe3 |
C |
T |
11: 69,039,429 (GRCm39) |
A667V |
probably benign |
Het |
Ank2 |
A |
G |
3: 126,749,601 (GRCm39) |
F476S |
probably damaging |
Het |
Aplp2 |
T |
A |
9: 31,063,637 (GRCm39) |
E657V |
possibly damaging |
Het |
Aspa |
G |
T |
11: 73,213,013 (GRCm39) |
L110I |
probably benign |
Het |
Atp6v1g3 |
A |
G |
1: 138,201,582 (GRCm39) |
K27E |
possibly damaging |
Het |
Aurkb |
C |
T |
11: 68,938,692 (GRCm39) |
R44W |
probably damaging |
Het |
Aurkb |
T |
C |
11: 68,938,696 (GRCm39) |
F45S |
probably benign |
Het |
B9d1 |
A |
T |
11: 61,396,029 (GRCm39) |
|
probably benign |
Het |
BC034090 |
A |
G |
1: 155,117,245 (GRCm39) |
I291T |
probably benign |
Het |
Borcs6 |
G |
A |
11: 68,951,453 (GRCm39) |
R277Q |
possibly damaging |
Het |
Btnl10 |
T |
C |
11: 58,810,138 (GRCm39) |
V93A |
probably benign |
Het |
Btnl10 |
C |
T |
11: 58,817,650 (GRCm39) |
T250I |
unknown |
Het |
Btnl10 |
AGAC |
AGACGAC |
11: 58,814,755 (GRCm39) |
|
probably benign |
Het |
Btnl10 |
AAAGA |
AAAGAAGA |
11: 58,814,753 (GRCm39) |
|
probably benign |
Het |
Ccdc42 |
C |
T |
11: 68,478,017 (GRCm39) |
|
probably benign |
Het |
Ccdc92b |
A |
G |
11: 74,520,880 (GRCm39) |
M61V |
possibly damaging |
Het |
Chd3 |
C |
A |
11: 69,239,271 (GRCm39) |
E1753D |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,252,277 (GRCm39) |
W42R |
probably benign |
Het |
Chrna9 |
T |
C |
5: 66,134,123 (GRCm39) |
F325L |
probably benign |
Het |
Clec3a |
G |
A |
8: 115,144,859 (GRCm39) |
V12M |
possibly damaging |
Het |
Cluh |
GCCTGA |
GCCTGATCCTGA |
11: 74,560,346 (GRCm39) |
|
probably benign |
Het |
Cluh |
CGAGCCTGAGCCTGAGCC |
CGAGCCTGAGCCTGAGCCTGAGCC |
11: 74,560,343 (GRCm39) |
|
probably benign |
Het |
Cluh |
CCCCGAGCC |
CCCCGAGCCCGAGCC |
11: 74,560,340 (GRCm39) |
|
probably benign |
Het |
Cluh |
TGAGCC |
TGAGCCCGAGCC |
11: 74,560,355 (GRCm39) |
|
probably benign |
Het |
Cluh |
G |
GGGCCTA |
11: 74,560,350 (GRCm39) |
|
probably benign |
Het |
Cluh |
CCTGAG |
CCTGAGTCTGAG |
11: 74,560,347 (GRCm39) |
|
probably benign |
Het |
Cluh |
CCGAGCC |
CCGAGCCCGAGCC |
11: 74,560,342 (GRCm39) |
|
probably benign |
Het |
Cnot9 |
T |
A |
1: 74,556,285 (GRCm39) |
N27K |
probably benign |
Het |
Cntrob |
C |
T |
11: 69,196,404 (GRCm39) |
R677H |
probably benign |
Het |
Cntrob |
G |
A |
11: 69,198,882 (GRCm39) |
P622L |
probably benign |
Het |
Crybg3 |
C |
T |
16: 59,326,608 (GRCm39) |
V1041M |
probably damaging |
Het |
Cyb5d1 |
C |
A |
11: 69,286,098 (GRCm39) |
A8S |
probably benign |
Het |
Cyb5d1 |
A |
G |
11: 69,286,028 (GRCm39) |
L31P |
probably benign |
Het |
Dnah9 |
G |
A |
11: 66,038,207 (GRCm39) |
H110Y |
probably benign |
Het |
Dnah9 |
A |
C |
11: 65,976,000 (GRCm39) |
S1350A |
probably benign |
Het |
Eif2b5 |
C |
T |
16: 20,317,671 (GRCm39) |
A3V |
unknown |
Het |
Elac2 |
T |
C |
11: 64,870,015 (GRCm39) |
S27P |
probably benign |
Het |
Epn2 |
C |
A |
11: 61,470,460 (GRCm39) |
|
probably benign |
Het |
Fam114a2 |
G |
A |
11: 57,380,940 (GRCm39) |
A438V |
probably benign |
Het |
Fam114a2 |
C |
T |
11: 57,390,581 (GRCm39) |
V318I |
probably benign |
Het |
Fam114a2 |
T |
C |
11: 57,390,623 (GRCm39) |
N304D |
probably benign |
Het |
Fam114a2 |
C |
T |
11: 57,405,060 (GRCm39) |
G14E |
probably benign |
Het |
Fam114a2 |
A |
G |
11: 57,374,858 (GRCm39) |
S494P |
probably benign |
Het |
Fam83g |
G |
A |
11: 61,594,020 (GRCm39) |
R518Q |
probably benign |
Het |
Fbxw10 |
G |
C |
11: 62,738,118 (GRCm39) |
R4T |
probably benign |
Het |
Fbxw10 |
G |
A |
11: 62,767,671 (GRCm39) |
V836I |
probably benign |
Het |
Foxo6 |
C |
T |
4: 120,144,332 (GRCm39) |
G40R |
possibly damaging |
Het |
Fsd1 |
C |
A |
17: 56,300,920 (GRCm39) |
P260T |
probably benign |
Het |
Galnt10 |
G |
A |
11: 57,656,514 (GRCm39) |
V233I |
probably benign |
Het |
Gemin5 |
T |
C |
11: 58,016,044 (GRCm39) |
S1321G |
probably benign |
Het |
Gemin5 |
T |
C |
11: 58,020,897 (GRCm39) |
M1097V |
probably benign |
Het |
Gemin5 |
C |
G |
11: 58,030,336 (GRCm39) |
A830P |
probably benign |
Het |
Gemin5 |
C |
G |
11: 58,030,401 (GRCm39) |
C808S |
probably benign |
Het |
Gemin5 |
C |
G |
11: 58,037,345 (GRCm39) |
E623D |
probably benign |
Het |
Gemin5 |
C |
G |
11: 58,013,115 (GRCm39) |
S1446T |
probably benign |
Het |
Ggnbp2 |
C |
T |
11: 84,727,478 (GRCm39) |
R481Q |
probably benign |
Het |
Gjc2 |
ACCCTCCCT |
ACCCTCCCTCCCT |
11: 59,073,561 (GRCm39) |
|
probably benign |
Het |
Gjc2 |
T |
C |
11: 59,067,259 (GRCm39) |
S408G |
unknown |
Het |
Glod4 |
A |
G |
11: 76,133,836 (GRCm39) |
V6A |
probably benign |
Het |
Glod4 |
T |
C |
11: 76,134,430 (GRCm39) |
K14R |
probably benign |
Het |
Glod4 |
C |
A |
11: 76,133,819 (GRCm39) |
|
probably null |
Het |
Glod4 |
T |
C |
11: 76,134,431 (GRCm39) |
K14E |
probably benign |
Het |
Glp2r |
C |
A |
11: 67,600,470 (GRCm39) |
V460F |
probably benign |
Het |
Glp2r |
C |
G |
11: 67,600,472 (GRCm39) |
G459A |
probably benign |
Het |
Glp2r |
C |
T |
11: 67,630,993 (GRCm39) |
V295I |
probably benign |
Het |
Glp2r |
A |
G |
11: 67,631,878 (GRCm39) |
V283A |
probably benign |
Het |
Glp2r |
T |
C |
11: 67,631,885 (GRCm39) |
I281V |
probably benign |
Het |
Glp2r |
T |
C |
11: 67,633,129 (GRCm39) |
T235A |
probably benign |
Het |
Glp2r |
A |
G |
11: 67,635,773 (GRCm39) |
V189A |
probably benign |
Het |
Glp2r |
C |
A |
11: 67,661,662 (GRCm39) |
A13S |
probably benign |
Het |
Glp2r |
C |
A |
11: 67,600,394 (GRCm39) |
R485L |
probably damaging |
Het |
Gm12253 |
A |
G |
11: 58,325,658 (GRCm39) |
E43G |
probably benign |
Het |
Gm12253 |
A |
C |
11: 58,325,686 (GRCm39) |
E52D |
probably benign |
Het |
Gm12253 |
A |
C |
11: 58,326,237 (GRCm39) |
E84A |
probably benign |
Het |
Gm12253 |
G |
A |
11: 58,326,309 (GRCm39) |
S108N |
probably benign |
Het |
Gm12253 |
G |
A |
11: 58,331,835 (GRCm39) |
A215T |
possibly damaging |
Het |
Gm12253 |
G |
C |
11: 58,325,367 (GRCm39) |
S13T |
possibly damaging |
Het |
Gm12258 |
G |
A |
11: 58,749,776 (GRCm39) |
G317E |
unknown |
Het |
Gm12258 |
A |
T |
11: 58,749,833 (GRCm39) |
E336V |
unknown |
Het |
Gm12258 |
A |
G |
11: 58,750,013 (GRCm39) |
|
probably benign |
Het |
Gm12258 |
T |
A |
11: 58,750,014 (GRCm39) |
|
probably benign |
Het |
Gm12258 |
G |
C |
11: 58,750,690 (GRCm39) |
G622R |
unknown |
Het |
Gm12258 |
T |
G |
11: 58,749,126 (GRCm39) |
S100R |
|
Het |
Gm12258 |
C |
T |
11: 58,749,262 (GRCm39) |
R146W |
|
Het |
Gm12258 |
G |
A |
11: 58,749,764 (GRCm39) |
R313H |
unknown |
Het |
Golga5 |
A |
G |
12: 102,440,853 (GRCm39) |
E196G |
probably benign |
Het |
Gps2 |
C |
T |
11: 69,807,130 (GRCm39) |
A60V |
probably benign |
Het |
Gucy2e |
C |
G |
11: 69,127,429 (GRCm39) |
G15R |
unknown |
Het |
Gucy2e |
C |
A |
11: 69,114,431 (GRCm39) |
A1033S |
probably benign |
Het |
Guk1 |
G |
A |
11: 59,082,747 (GRCm39) |
|
probably benign |
Het |
Haspin |
A |
G |
11: 73,028,777 (GRCm39) |
L104P |
probably benign |
Het |
Haspin |
T |
C |
11: 73,028,174 (GRCm39) |
Q305R |
probably benign |
Het |
Hes7 |
T |
C |
11: 69,013,782 (GRCm39) |
S214P |
probably benign |
Het |
Hic1 |
G |
A |
11: 75,058,352 (GRCm39) |
T179M |
probably damaging |
Het |
Iba57 |
AG |
AGCG |
11: 59,052,330 (GRCm39) |
|
probably null |
Het |
Iba57 |
CAGA |
CAGAGA |
11: 59,052,329 (GRCm39) |
|
probably null |
Het |
Iba57 |
C |
G |
11: 59,053,865 (GRCm39) |
G36R |
unknown |
Het |
Iba57 |
T |
C |
11: 59,052,384 (GRCm39) |
T86A |
unknown |
Het |
Iba57 |
T |
C |
11: 59,052,381 (GRCm39) |
T87A |
unknown |
Het |
Ifi207 |
G |
A |
1: 173,558,093 (GRCm39) |
T215I |
unknown |
Het |
Iftap |
T |
C |
2: 101,440,950 (GRCm39) |
K18E |
probably benign |
Het |
Igtp |
T |
G |
11: 58,097,169 (GRCm39) |
D113E |
probably damaging |
Het |
Igtp |
C |
G |
11: 58,097,944 (GRCm39) |
L372V |
probably benign |
Het |
Igtp |
C |
G |
11: 58,097,791 (GRCm39) |
L321V |
possibly damaging |
Het |
Irgm2 |
A |
G |
11: 58,110,389 (GRCm39) |
N27D |
probably benign |
Het |
Irgm2 |
T |
A |
11: 58,110,339 (GRCm39) |
V10D |
probably benign |
Het |
Irgm2 |
C |
G |
11: 58,111,389 (GRCm39) |
T360S |
probably benign |
Het |
Irgm2 |
G |
T |
11: 58,111,238 (GRCm39) |
A310S |
possibly damaging |
Het |
Irgm2 |
A |
C |
11: 58,110,951 (GRCm39) |
H214P |
probably benign |
Het |
Irgm2 |
G |
A |
11: 58,110,924 (GRCm39) |
S205N |
probably benign |
Het |
Irgm2 |
G |
A |
11: 58,110,833 (GRCm39) |
V175I |
probably benign |
Het |
Irgm2 |
T |
C |
11: 58,110,780 (GRCm39) |
L157S |
probably benign |
Het |
Irgm2 |
T |
C |
11: 58,110,738 (GRCm39) |
I143T |
probably benign |
Het |
Itgae |
T |
A |
11: 72,994,713 (GRCm39) |
L22M |
possibly damaging |
Het |
Itgae |
C |
G |
11: 73,024,953 (GRCm39) |
S1028W |
probably benign |
Het |
Itgae |
G |
T |
11: 73,012,783 (GRCm39) |
G705V |
probably benign |
Het |
Itgae |
A |
T |
11: 73,012,757 (GRCm39) |
K696N |
probably benign |
Het |
Itgae |
G |
A |
11: 73,008,913 (GRCm39) |
V465I |
probably benign |
Het |
Itgae |
A |
G |
11: 73,006,466 (GRCm39) |
H378R |
probably benign |
Het |
Itgae |
A |
T |
11: 72,994,786 (GRCm39) |
Q46L |
probably damaging |
Het |
Kif1c |
C |
T |
11: 70,614,940 (GRCm39) |
P578L |
probably benign |
Het |
Klhdc7a |
A |
G |
4: 139,693,852 (GRCm39) |
I365T |
probably damaging |
Het |
Kmt2d |
T |
C |
15: 98,749,625 (GRCm39) |
N2656D |
unknown |
Het |
Larp1 |
G |
A |
11: 57,933,166 (GRCm39) |
V257I |
probably benign |
Het |
Llgl1 |
ACCCCAGCCCTTCTGATTACTGCCCTCCCCAGC |
ACCCCAGC |
11: 60,603,923 (GRCm39) |
|
probably null |
Het |
Lrp1b |
A |
T |
2: 40,640,946 (GRCm39) |
N3499K |
|
Het |
Lypd8 |
C |
A |
11: 58,275,475 (GRCm39) |
A70E |
possibly damaging |
Het |
Lypd8 |
G |
A |
11: 58,275,489 (GRCm39) |
E75K |
probably benign |
Het |
Lypd8 |
CAATCACCAACA |
CAATCACCAACAGTTCCCTCGCCTCTGTTACCCCACAAATCACCAACA |
11: 58,281,059 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
T |
C |
11: 58,273,601 (GRCm39) |
Y27H |
probably benign |
Het |
Lypd8l |
T |
G |
11: 58,503,397 (GRCm39) |
S44R |
probably benign |
Het |
Lypd8l |
G |
A |
11: 58,499,335 (GRCm39) |
P161L |
probably benign |
Het |
Lypd8l |
A |
G |
11: 58,503,387 (GRCm39) |
L47P |
probably benign |
Het |
Mapk7 |
CGCTGGTGCTGG |
CGCTGGTGCTGGTGCTGG |
11: 61,381,038 (GRCm39) |
|
probably benign |
Het |
Mapk7 |
TGGGGCAGGGGCAGGGGCAGG |
TGGCGCTGGGGCAGGGGCAGGGGCAGGGGCAGG |
11: 61,381,053 (GRCm39) |
|
probably benign |
Het |
Mfap3 |
A |
T |
11: 57,418,866 (GRCm39) |
I9F |
possibly damaging |
Het |
Mfap3 |
G |
A |
11: 57,418,902 (GRCm39) |
G21S |
probably benign |
Het |
Mrm3 |
G |
A |
11: 76,134,903 (GRCm39) |
R102K |
probably benign |
Het |
Mrm3 |
C |
T |
11: 76,138,221 (GRCm39) |
P203L |
probably benign |
Het |
Mrpl22 |
G |
A |
11: 58,062,521 (GRCm39) |
A4T |
unknown |
Het |
Mrpl55 |
A |
G |
11: 59,094,999 (GRCm39) |
|
probably null |
Het |
Mrpl55 |
A |
T |
11: 59,095,415 (GRCm39) |
L26F |
probably benign |
Het |
Myh1 |
A |
C |
11: 67,095,272 (GRCm39) |
T211P |
probably benign |
Het |
Myh8 |
A |
C |
11: 67,188,312 (GRCm39) |
N991T |
probably benign |
Het |
Myo18a |
C |
A |
11: 77,744,643 (GRCm39) |
F1970L |
possibly damaging |
Het |
Myocd |
A |
G |
11: 65,075,418 (GRCm39) |
S697P |
probably benign |
Het |
Nlgn2 |
A |
G |
11: 69,719,220 (GRCm39) |
V210A |
possibly damaging |
Het |
Nlrp1a |
T |
C |
11: 70,983,069 (GRCm39) |
K1299R |
probably benign |
Het |
Nlrp1a |
C |
T |
11: 70,988,077 (GRCm39) |
R1131Q |
probably damaging |
Het |
Nlrp1a |
T |
C |
11: 70,990,442 (GRCm39) |
I1038V |
probably benign |
Het |
Nlrp1a |
T |
C |
11: 71,014,914 (GRCm39) |
E112G |
probably benign |
Het |
Nlrp1a |
C |
G |
11: 71,033,355 (GRCm39) |
|
probably null |
Het |
Nlrp1b |
A |
G |
11: 71,072,625 (GRCm39) |
I406T |
probably benign |
Het |
Nlrp1b |
A |
G |
11: 71,073,148 (GRCm39) |
Y232H |
probably benign |
Het |
Nlrp1b |
A |
T |
11: 71,073,266 (GRCm39) |
D192E |
probably benign |
Het |
Nlrp1b |
T |
C |
11: 71,073,280 (GRCm39) |
T188A |
probably benign |
Het |
Nlrp1b |
C |
G |
11: 71,073,370 (GRCm39) |
E158Q |
probably benign |
Het |
Nlrp1b |
A |
T |
11: 71,073,378 (GRCm39) |
M155K |
probably benign |
Het |
Nlrp1b |
T |
A |
11: 71,073,396 (GRCm39) |
Q149L |
probably benign |
Het |
Nlrp1b |
T |
C |
11: 71,073,503 (GRCm39) |
I113M |
probably benign |
Het |
Nlrp1b |
C |
A |
11: 71,072,534 (GRCm39) |
M436I |
probably benign |
Het |
Nlrp1b |
A |
C |
11: 71,072,539 (GRCm39) |
S435A |
probably benign |
Het |
Nmur2 |
T |
C |
11: 55,931,104 (GRCm39) |
I202M |
probably benign |
Het |
Obscn |
C |
G |
11: 58,970,722 (GRCm39) |
V2328L |
probably benign |
Het |
Obscn |
C |
A |
11: 58,972,698 (GRCm39) |
G2116V |
possibly damaging |
Het |
Obscn |
C |
T |
11: 58,977,505 (GRCm39) |
R1865H |
probably benign |
Het |
Obscn |
T |
C |
11: 58,977,527 (GRCm39) |
R1858G |
probably benign |
Het |
Obscn |
A |
G |
11: 58,977,565 (GRCm39) |
V1845A |
probably benign |
Het |
Obscn |
A |
G |
11: 58,984,142 (GRCm39) |
F1771S |
probably benign |
Het |
Obscn |
C |
T |
11: 58,984,239 (GRCm39) |
V1739M |
possibly damaging |
Het |
Obscn |
G |
T |
11: 58,984,334 (GRCm39) |
A1707D |
possibly damaging |
Het |
Obscn |
C |
T |
11: 58,984,335 (GRCm39) |
A1707T |
probably benign |
Het |
Obscn |
G |
A |
11: 58,984,385 (GRCm39) |
A1690V |
probably benign |
Het |
Obscn |
C |
T |
11: 58,990,735 (GRCm39) |
A1613T |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,990,755 (GRCm39) |
H1606R |
probably benign |
Het |
Obscn |
C |
G |
11: 58,994,167 (GRCm39) |
A1572P |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,994,340 (GRCm39) |
H1514R |
probably benign |
Het |
Obscn |
G |
A |
11: 58,994,364 (GRCm39) |
A1506V |
probably benign |
Het |
Obscn |
T |
C |
11: 59,003,380 (GRCm39) |
E1306G |
probably benign |
Het |
Obscn |
T |
C |
11: 59,013,563 (GRCm39) |
M1095V |
probably benign |
Het |
Obscn |
C |
T |
11: 59,018,892 (GRCm39) |
A949T |
probably benign |
Het |
Obscn |
C |
T |
11: 59,018,895 (GRCm39) |
V973M |
probably damaging |
Het |
Obscn |
G |
T |
11: 59,020,663 (GRCm39) |
L794M |
probably benign |
Het |
Obscn |
C |
T |
11: 59,021,449 (GRCm39) |
R797H |
probably damaging |
Het |
Obscn |
C |
T |
11: 59,023,937 (GRCm39) |
A578T |
possibly damaging |
Het |
Obscn |
G |
A |
11: 59,024,066 (GRCm39) |
P535S |
probably damaging |
Het |
Obscn |
C |
G |
11: 59,024,072 (GRCm39) |
A533P |
probably benign |
Het |
Obscn |
T |
C |
11: 59,026,505 (GRCm39) |
I233V |
probably benign |
Het |
Obscn |
C |
T |
11: 58,940,306 (GRCm39) |
D5354N |
|
Het |
Obscn |
C |
A |
11: 58,940,614 (GRCm39) |
R4593S |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,940,623 (GRCm39) |
T5307A |
|
Het |
Obscn |
G |
A |
11: 58,942,383 (GRCm39) |
T4372M |
probably benign |
Het |
Obscn |
T |
C |
11: 58,943,439 (GRCm39) |
M4237V |
probably benign |
Het |
Obscn |
C |
T |
11: 58,944,594 (GRCm39) |
R4700Q |
probably benign |
Het |
Obscn |
T |
C |
11: 58,944,651 (GRCm39) |
K4681R |
probably benign |
Het |
Obscn |
T |
C |
11: 58,945,044 (GRCm39) |
E4658G |
probably benign |
Het |
Obscn |
C |
T |
11: 58,945,176 (GRCm39) |
R4614Q |
probably benign |
Het |
Obscn |
T |
C |
11: 58,946,331 (GRCm39) |
D4458G |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,946,340 (GRCm39) |
R4455K |
probably benign |
Het |
Obscn |
G |
T |
11: 58,946,936 (GRCm39) |
A4066E |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,947,595 (GRCm39) |
M4478T |
|
Het |
Obscn |
C |
A |
11: 58,951,823 (GRCm39) |
G3977W |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,952,388 (GRCm39) |
G3894R |
probably benign |
Het |
Obscn |
CCACACACACACAC |
CCACACACACAC |
11: 58,954,279 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,954,300 (GRCm39) |
T4037A |
|
Het |
Obscn |
T |
C |
11: 58,954,402 (GRCm39) |
K3727E |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,957,973 (GRCm39) |
R3576C |
probably benign |
Het |
Obscn |
C |
T |
11: 58,958,655 (GRCm39) |
V3433I |
probably benign |
Het |
Obscn |
G |
A,C |
11: 58,960,659 (GRCm39) |
|
silent |
Het |
Obscn |
C |
A |
11: 58,960,757 (GRCm39) |
A3185S |
probably benign |
Het |
Obscn |
C |
T |
11: 58,967,334 (GRCm39) |
V2792I |
possibly damaging |
Het |
Obscn |
G |
A |
11: 58,891,715 (GRCm39) |
A6939V |
probably benign |
Het |
Obscn |
C |
G |
11: 58,900,019 (GRCm39) |
G938A |
probably benign |
Het |
Obscn |
G |
C |
11: 58,904,014 (GRCm39) |
T7320S |
probably benign |
Het |
Obscn |
C |
T |
11: 58,921,934 (GRCm39) |
R5954Q |
probably damaging |
Het |
Obscn |
G |
C |
11: 58,929,976 (GRCm39) |
P5080A |
probably benign |
Het |
Obscn |
T |
A |
11: 58,929,990 (GRCm39) |
Q5075L |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,932,601 (GRCm39) |
I4869V |
probably benign |
Het |
Obscn |
T |
C |
11: 58,933,776 (GRCm39) |
T5363A |
probably benign |
Het |
Obscn |
G |
A |
11: 58,933,853 (GRCm39) |
A5337V |
probably benign |
Het |
Obscn |
G |
A |
11: 58,933,878 (GRCm39) |
R5329C |
probably benign |
Het |
Obscn |
G |
A |
11: 58,969,984 (GRCm39) |
R53C |
probably damaging |
Het |
Or11l3 |
A |
C |
11: 58,516,732 (GRCm39) |
C46G |
possibly damaging |
Het |
Or11l3 |
T |
G |
11: 58,516,619 (GRCm39) |
K84N |
probably benign |
Het |
Or11l3 |
G |
A |
11: 58,516,588 (GRCm39) |
P95S |
probably benign |
Het |
Or11l3 |
C |
G |
11: 58,516,130 (GRCm39) |
G61R |
probably benign |
Het |
Or11l3 |
G |
A |
11: 58,516,075 (GRCm39) |
S79F |
probably benign |
Het |
Or14j10 |
A |
G |
17: 37,934,735 (GRCm39) |
S264P |
probably damaging |
Het |
Or2ab1 |
A |
C |
11: 58,488,344 (GRCm39) |
I35L |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,776 (GRCm39) |
S179G |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,491 (GRCm39) |
S84G |
possibly damaging |
Het |
Or2ab1 |
A |
G |
11: 58,488,356 (GRCm39) |
I39V |
probably benign |
Het |
Or2ak4 |
G |
A |
11: 58,648,793 (GRCm39) |
A101T |
probably benign |
Het |
Or2ak4 |
A |
C |
11: 58,649,186 (GRCm39) |
K232Q |
probably benign |
Het |
Or2ak4 |
A |
C |
11: 58,649,168 (GRCm39) |
I226L |
probably benign |
Het |
Or2ak4 |
G |
A |
11: 58,649,153 (GRCm39) |
V221M |
probably damaging |
Het |
Or2ak4 |
A |
G |
11: 58,648,931 (GRCm39) |
S147G |
probably benign |
Het |
Or2ak4 |
C |
T |
11: 58,648,895 (GRCm39) |
L135F |
probably benign |
Het |
Or2ak5 |
G |
A |
11: 58,611,922 (GRCm39) |
|
probably benign |
Het |
Or2ak6 |
C |
A |
11: 58,593,222 (GRCm39) |
Q232K |
probably benign |
Het |
Or2ak6 |
C |
T |
11: 58,593,153 (GRCm39) |
L209F |
possibly damaging |
Het |
Or2ak6 |
A |
C |
11: 58,592,784 (GRCm39) |
I86L |
probably benign |
Het |
Or2ak7 |
G |
T |
11: 58,574,758 (GRCm39) |
D20Y |
probably benign |
Het |
Or2ak7 |
T |
C |
11: 58,575,548 (GRCm39) |
L283P |
probably benign |
Het |
Or2ak7 |
C |
T |
11: 58,575,289 (GRCm39) |
H197Y |
probably benign |
Het |
Or2ak7 |
G |
A |
11: 58,575,083 (GRCm39) |
R128Q |
probably benign |
Het |
Or2ak7 |
G |
A |
11: 58,574,941 (GRCm39) |
V81M |
probably benign |
Het |
Or2ak7 |
T |
C |
11: 58,574,815 (GRCm39) |
F39L |
probably benign |
Het |
Or2av9 |
C |
A |
11: 58,380,574 (GRCm39) |
E336* |
probably null |
Het |
Or2av9 |
T |
C |
11: 58,381,314 (GRCm39) |
Q89R |
probably benign |
Het |
Or2av9 |
C |
T |
11: 58,381,123 (GRCm39) |
A153T |
probably benign |
Het |
Or2t29 |
G |
T |
11: 58,434,272 (GRCm39) |
S23Y |
probably benign |
Het |
Or2t43 |
G |
A |
11: 58,457,388 (GRCm39) |
A261V |
probably benign |
Het |
Or2t43 |
C |
T |
11: 58,457,920 (GRCm39) |
V84I |
probably benign |
Het |
Or2t43 |
A |
T |
11: 58,457,521 (GRCm39) |
S217T |
probably benign |
Het |
Or2t44 |
A |
G |
11: 58,677,773 (GRCm39) |
T238A |
probably damaging |
Het |
Or2t46 |
T |
G |
11: 58,472,122 (GRCm39) |
L151V |
probably benign |
Het |
Or2t46 |
G |
A |
11: 58,471,828 (GRCm39) |
V53I |
probably benign |
Het |
Or2t46 |
T |
C |
11: 58,471,757 (GRCm39) |
V29A |
probably benign |
Het |
Or2t46 |
G |
C |
11: 58,472,483 (GRCm39) |
S271T |
probably benign |
Het |
Or2t46 |
C |
T |
11: 58,471,750 (GRCm39) |
H27Y |
probably benign |
Het |
Or2t47 |
T |
C |
11: 58,442,387 (GRCm39) |
K226R |
probably benign |
Het |
Or2t47 |
C |
T |
11: 58,442,801 (GRCm39) |
S88N |
probably benign |
Het |
Or2t47 |
C |
T |
11: 58,442,940 (GRCm39) |
A42T |
probably benign |
Het |
Or2t49 |
T |
C |
11: 58,392,927 (GRCm39) |
I158V |
probably benign |
Het |
Or2t49 |
C |
A |
11: 58,392,936 (GRCm39) |
V155F |
probably benign |
Het |
Or2t49 |
GGTGGATTGGTATGTGGAT |
GGTGGAT |
11: 58,393,212 (GRCm39) |
|
probably benign |
Het |
Or2t49 |
C |
G |
11: 58,393,287 (GRCm39) |
V38L |
probably benign |
Het |
Or2t49 |
C |
T |
11: 58,393,396 (GRCm39) |
M1I |
probably null |
Het |
Or2t49 |
T |
C |
11: 58,392,474 (GRCm39) |
M309V |
probably benign |
Het |
Or2w3 |
T |
G |
11: 58,557,342 (GRCm39) |
I319R |
probably benign |
Het |
Or2w3b |
G |
A |
11: 58,623,295 (GRCm39) |
A232V |
probably benign |
Het |
Or2w3b |
T |
C |
11: 58,623,475 (GRCm39) |
H172R |
probably benign |
Het |
Or2w3b |
C |
A |
11: 58,624,048 (GRCm39) |
|
probably benign |
Het |
Or2w3b |
T |
G |
11: 58,623,200 (GRCm39) |
N264H |
probably benign |
Het |
Or5af2 |
T |
C |
11: 58,708,122 (GRCm39) |
V96A |
probably benign |
Het |
Or5af2 |
A |
C |
11: 58,708,220 (GRCm39) |
I129L |
probably benign |
Het |
Or5af2 |
C |
G |
11: 58,708,243 (GRCm39) |
H136Q |
probably benign |
Het |
Or5af2 |
T |
C |
11: 58,708,508 (GRCm39) |
C225R |
probably benign |
Het |
Or5af2 |
C |
G |
11: 58,708,644 (GRCm39) |
P270R |
probably benign |
Het |
Or5af2 |
A |
G |
11: 58,707,887 (GRCm39) |
I18V |
probably benign |
Het |
Or6k2 |
C |
A |
1: 173,986,907 (GRCm39) |
C189* |
probably null |
Het |
Or9e1 |
G |
T |
11: 58,731,945 (GRCm39) |
A2S |
probably benign |
Het |
Or9e1 |
G |
C |
11: 58,731,907 (GRCm39) |
|
probably benign |
Het |
Or9e1 |
A |
G |
11: 58,732,615 (GRCm39) |
H225R |
probably benign |
Het |
Or9e1 |
G |
A |
11: 58,732,569 (GRCm39) |
A210T |
probably benign |
Het |
Or9e1 |
C |
T |
11: 58,732,032 (GRCm39) |
L31F |
probably benign |
Het |
Or9e1 |
T |
C |
11: 58,732,084 (GRCm39) |
I48T |
probably benign |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Ovca2 |
T |
C |
11: 75,069,528 (GRCm39) |
T32A |
probably benign |
Het |
Pfkfb1 |
T |
G |
X: 149,391,627 (GRCm39) |
V25G |
probably damaging |
Het |
Pimreg |
G |
A |
11: 71,935,979 (GRCm39) |
R154H |
probably damaging |
Het |
Pimreg |
TCACA |
TCA |
11: 71,935,801 (GRCm39) |
|
probably benign |
Het |
Pitpnm3 |
C |
T |
11: 72,010,969 (GRCm39) |
R21Q |
probably benign |
Het |
Pitpnm3 |
T |
C |
11: 71,954,955 (GRCm39) |
K520E |
probably benign |
Het |
Ppp1r12b |
C |
G |
1: 134,883,262 (GRCm39) |
V87L |
probably benign |
Het |
Pramel13 |
A |
G |
4: 144,122,517 (GRCm39) |
L9P |
probably damaging |
Het |
Prpsap2 |
A |
C |
11: 61,647,078 (GRCm39) |
V21G |
possibly damaging |
Het |
Rabep1 |
C |
CT |
11: 70,830,910 (GRCm39) |
|
probably null |
Het |
Rai1 |
A |
G |
11: 60,078,389 (GRCm39) |
N818D |
probably benign |
Het |
Rap1gap2 |
C |
T |
11: 74,487,721 (GRCm39) |
E52K |
probably benign |
Het |
Rc3h2 |
T |
C |
2: 37,289,612 (GRCm39) |
H400R |
possibly damaging |
Het |
Rnf112 |
A |
G |
11: 61,341,775 (GRCm39) |
L343P |
unknown |
Het |
Rnf167 |
C |
CACAGGGA |
11: 70,541,646 (GRCm39) |
|
probably null |
Het |
Rtn4rl1 |
C |
T |
11: 75,156,863 (GRCm39) |
P432S |
probably benign |
Het |
Shisa6 |
CGCCGC |
CGCCGCAGCCGC |
11: 66,416,533 (GRCm39) |
|
probably benign |
Het |
Shisa6 |
CGCCGC |
CGCCGCGGCCGC |
11: 66,416,524 (GRCm39) |
|
probably benign |
Het |
Slc2a4 |
GGCCG |
GG |
11: 69,834,818 (GRCm39) |
|
probably benign |
Het |
Slc2a4 |
GCC |
G |
11: 69,834,819 (GRCm39) |
|
probably null |
Het |
Slc6a4 |
G |
A |
11: 76,901,382 (GRCm39) |
G39E |
probably benign |
Het |
Slc6a4 |
A |
G |
11: 76,903,858 (GRCm39) |
K152R |
probably benign |
Het |
Smcr8 |
T |
C |
11: 60,669,932 (GRCm39) |
V360A |
probably benign |
Het |
Smcr8 |
A |
G |
11: 60,668,806 (GRCm39) |
|
probably benign |
Het |
Smcr8 |
C |
A |
11: 60,670,699 (GRCm39) |
R616S |
probably benign |
Het |
Smg6 |
G |
T |
11: 75,047,092 (GRCm39) |
A1262S |
probably benign |
Het |
Spata31h1 |
CGAATCTGCACACTGAGGACTTGGCCCTGGGATGCATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGGATGCATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGGATGCATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGGATGTATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGG |
CGAATCTGCACACTGAGGACTTGGCCCTGGGATGCATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGGATGCATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGGATGTATGCAGGAGAATCTGCACACTGAGGACTTGGCCCTGGG |
10: 82,124,390 (GRCm39) |
|
probably benign |
Het |
Spns3 |
G |
A |
11: 72,440,917 (GRCm39) |
P40S |
probably benign |
Het |
Spns3 |
T |
C |
11: 72,440,863 (GRCm39) |
I58V |
probably benign |
Het |
Spns3 |
T |
C |
11: 72,440,986 (GRCm39) |
S17G |
probably benign |
Het |
Srebf1 |
C |
T |
11: 60,097,061 (GRCm39) |
V256M |
probably benign |
Het |
Tekt1 |
T |
C |
11: 72,250,597 (GRCm39) |
Q33R |
probably benign |
Het |
Timm22 |
T |
G |
11: 76,297,943 (GRCm39) |
V18G |
probably benign |
Het |
Tmem102 |
C |
G |
11: 69,695,902 (GRCm39) |
G53A |
possibly damaging |
Het |
Tmem102 |
G |
C |
11: 69,695,927 (GRCm39) |
R45G |
probably benign |
Het |
Tmem11 |
A |
G |
11: 60,766,658 (GRCm39) |
|
probably benign |
Het |
Tom1l2 |
C |
T |
11: 60,132,682 (GRCm39) |
A414T |
probably benign |
Het |
Tomm20l |
ACAAGATTC |
AC |
12: 71,168,758 (GRCm39) |
|
probably null |
Het |
Top3a |
C |
T |
11: 60,641,410 (GRCm39) |
G425S |
probably benign |
Het |
Trim16 |
T |
C |
11: 62,731,572 (GRCm39) |
V481A |
probably benign |
Het |
Trim16 |
G |
A |
11: 62,727,643 (GRCm39) |
E322K |
probably benign |
Het |
Trim16 |
A |
AAGC |
11: 62,711,521 (GRCm39) |
|
probably benign |
Het |
Trim16 |
GA |
GAACA |
11: 62,711,520 (GRCm39) |
|
probably benign |
Het |
Trim16 |
TGAAGA |
TGAAGAAGA |
11: 62,711,516 (GRCm39) |
|
probably benign |
Het |
Trim16 |
G |
C |
11: 62,711,502 (GRCm39) |
V58L |
probably benign |
Het |
Trim16 |
C |
T |
11: 62,711,428 (GRCm39) |
A33V |
probably benign |
Het |
Trim16 |
C |
A |
11: 62,731,675 (GRCm39) |
D515E |
probably benign |
Het |
Trim17 |
G |
A |
11: 58,856,331 (GRCm39) |
M129I |
probably benign |
Het |
Trim17 |
A |
G |
11: 58,861,272 (GRCm39) |
N259S |
probably benign |
Het |
Trim23 |
G |
A |
13: 104,315,395 (GRCm39) |
A3T |
probably benign |
Het |
Trim58 |
A |
G |
11: 58,542,486 (GRCm39) |
N482S |
probably benign |
Het |
Trim58 |
C |
A |
11: 58,531,684 (GRCm39) |
L131M |
possibly damaging |
Het |
Trmt1l |
A |
G |
1: 151,333,331 (GRCm39) |
N642S |
possibly damaging |
Het |
Trpv1 |
C |
G |
11: 73,131,427 (GRCm39) |
P322A |
possibly damaging |
Het |
Trpv1 |
C |
A |
11: 73,145,117 (GRCm39) |
D734E |
probably benign |
Het |
Trpv3 |
G |
A |
11: 73,169,803 (GRCm39) |
A125T |
probably benign |
Het |
Trpv3 |
C |
T |
11: 73,160,513 (GRCm39) |
A9V |
probably benign |
Het |
Trpv3 |
A |
G |
11: 73,174,502 (GRCm39) |
T290A |
probably benign |
Het |
Tvp23b |
A |
C |
11: 62,772,769 (GRCm39) |
N7H |
possibly damaging |
Het |
Usp43 |
AGGGC |
AGGGCAGGGGATGAACCTCGGGC |
11: 67,746,545 (GRCm39) |
|
probably benign |
Het |
Usp43 |
C |
T |
11: 67,747,332 (GRCm39) |
G792S |
probably benign |
Het |
Vamp2 |
C |
T |
11: 68,979,411 (GRCm39) |
|
probably benign |
Het |
Vamp2 |
G |
A |
11: 68,980,889 (GRCm39) |
G124R |
possibly damaging |
Het |
Vmn2r15 |
G |
T |
5: 109,434,529 (GRCm39) |
P725H |
probably damaging |
Het |
Vmn2r18 |
T |
C |
5: 151,508,497 (GRCm39) |
D209G |
probably benign |
Het |
Wdr4 |
C |
T |
17: 31,731,177 (GRCm39) |
G61E |
probably damaging |
Het |
Xaf1 |
G |
C |
11: 72,199,856 (GRCm39) |
V198L |
unknown |
Het |
Xaf1 |
GGCT |
GGCTGGCCAGCT |
11: 72,199,846 (GRCm39) |
|
probably null |
Het |
Xaf1 |
T |
G |
11: 72,199,792 (GRCm39) |
C176W |
unknown |
Het |
Xaf1 |
A |
G |
11: 72,199,476 (GRCm39) |
E71G |
probably benign |
Het |
Xaf1 |
C |
A |
11: 72,197,434 (GRCm39) |
L137I |
probably benign |
Het |
Xaf1 |
G |
C |
11: 72,197,429 (GRCm39) |
C135S |
probably damaging |
Het |
Xaf1 |
G |
A |
11: 72,197,426 (GRCm39) |
R134H |
probably benign |
Het |
Xaf1 |
T |
C |
11: 72,199,881 (GRCm39) |
L206S |
unknown |
Het |
Zfhx4 |
C |
G |
3: 5,308,067 (GRCm39) |
S431C |
probably damaging |
Het |
Zfp286 |
G |
A |
11: 62,675,782 (GRCm39) |
T60M |
probably damaging |
Het |
Zfp286 |
A |
G |
11: 62,678,795 (GRCm39) |
V44A |
probably benign |
Het |
Zfp287 |
G |
A |
11: 62,613,757 (GRCm39) |
R225* |
probably null |
Het |
Zfp287 |
C |
T |
11: 62,604,633 (GRCm39) |
R758H |
probably benign |
Het |
Zfp287 |
C |
G |
11: 62,606,175 (GRCm39) |
C244S |
probably benign |
Het |
Zfp39 |
T |
C |
11: 58,781,526 (GRCm39) |
N412S |
possibly damaging |
Het |
Zfp39 |
T |
C |
11: 58,781,274 (GRCm39) |
D496G |
possibly damaging |
Het |
Zfp39 |
G |
C |
11: 58,781,273 (GRCm39) |
D496E |
probably benign |
Het |
Zfp39 |
G |
C |
11: 58,781,130 (GRCm39) |
T544R |
possibly damaging |
Het |
Zfp39 |
A |
C |
11: 58,780,873 (GRCm39) |
Y630D |
probably benign |
Het |
Zfp39 |
G |
C |
11: 58,780,871 (GRCm39) |
Y630* |
probably null |
Het |
Zfp39 |
T |
G |
11: 58,791,409 (GRCm39) |
S93R |
probably benign |
Het |
Zfp39 |
G |
T |
11: 58,791,407 (GRCm39) |
S93R |
probably benign |
Het |
Zfp39 |
T |
C |
11: 58,782,142 (GRCm39) |
K207E |
probably benign |
Het |
Zfp39 |
A |
G |
11: 58,782,123 (GRCm39) |
I213T |
probably benign |
Het |
Zfp39 |
T |
A |
11: 58,781,967 (GRCm39) |
H265L |
probably damaging |
Het |
Zfp39 |
G |
T |
11: 58,781,597 (GRCm39) |
N388K |
probably benign |
Het |
Zfp39 |
A |
G |
11: 58,781,605 (GRCm39) |
S386P |
probably benign |
Het |
Zfp39 |
A |
C |
11: 58,781,702 (GRCm39) |
H353Q |
probably damaging |
Het |
Zfp39 |
A |
C |
11: 58,781,712 (GRCm39) |
V350G |
probably benign |
Het |
Zfp39 |
A |
G |
11: 58,781,724 (GRCm39) |
V346A |
probably benign |
Het |
Zfp39 |
T |
A |
11: 58,781,751 (GRCm39) |
K337M |
probably benign |
Het |
Zfp672 |
G |
T |
11: 58,220,452 (GRCm39) |
T49K |
unknown |
Het |
Zfp692 |
G |
T |
11: 58,199,859 (GRCm39) |
E149D |
probably benign |
Het |
Zfp692 |
G |
A |
11: 58,200,844 (GRCm39) |
V242I |
probably benign |
Het |
Zzef1 |
G |
A |
11: 72,780,008 (GRCm39) |
R1927H |
probably benign |
Het |
|
Other mutations in Fat2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00720:Fat2
|
APN |
11 |
55,202,070 (GRCm39) |
missense |
probably benign |
|
IGL00897:Fat2
|
APN |
11 |
55,180,078 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01161:Fat2
|
APN |
11 |
55,175,017 (GRCm39) |
missense |
probably benign |
|
IGL01306:Fat2
|
APN |
11 |
55,201,698 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01393:Fat2
|
APN |
11 |
55,160,135 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01529:Fat2
|
APN |
11 |
55,172,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Fat2
|
APN |
11 |
55,174,213 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01555:Fat2
|
APN |
11 |
55,169,756 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01758:Fat2
|
APN |
11 |
55,187,035 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01768:Fat2
|
APN |
11 |
55,153,394 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01939:Fat2
|
APN |
11 |
55,174,806 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01941:Fat2
|
APN |
11 |
55,202,831 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01967:Fat2
|
APN |
11 |
55,202,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01978:Fat2
|
APN |
11 |
55,160,972 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01998:Fat2
|
APN |
11 |
55,187,021 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02001:Fat2
|
APN |
11 |
55,203,071 (GRCm39) |
start codon destroyed |
probably null |
0.89 |
IGL02004:Fat2
|
APN |
11 |
55,173,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02103:Fat2
|
APN |
11 |
55,180,122 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02131:Fat2
|
APN |
11 |
55,199,868 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02155:Fat2
|
APN |
11 |
55,153,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02223:Fat2
|
APN |
11 |
55,163,955 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02231:Fat2
|
APN |
11 |
55,171,918 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02312:Fat2
|
APN |
11 |
55,161,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02476:Fat2
|
APN |
11 |
55,201,950 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02539:Fat2
|
APN |
11 |
55,172,619 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02553:Fat2
|
APN |
11 |
55,202,109 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02645:Fat2
|
APN |
11 |
55,173,654 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Fat2
|
APN |
11 |
55,201,922 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Fat2
|
APN |
11 |
55,173,211 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02883:Fat2
|
APN |
11 |
55,147,444 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02894:Fat2
|
APN |
11 |
55,147,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02975:Fat2
|
APN |
11 |
55,161,020 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03085:Fat2
|
APN |
11 |
55,174,072 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03106:Fat2
|
APN |
11 |
55,202,727 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03132:Fat2
|
APN |
11 |
55,144,746 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03133:Fat2
|
APN |
11 |
55,176,869 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03194:Fat2
|
APN |
11 |
55,201,821 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03266:Fat2
|
APN |
11 |
55,174,855 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03290:Fat2
|
APN |
11 |
55,147,045 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03291:Fat2
|
APN |
11 |
55,153,421 (GRCm39) |
missense |
probably benign |
|
IGL03325:Fat2
|
APN |
11 |
55,173,168 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03345:Fat2
|
APN |
11 |
55,173,187 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03371:Fat2
|
APN |
11 |
55,201,990 (GRCm39) |
missense |
probably benign |
0.10 |
ANU23:Fat2
|
UTSW |
11 |
55,201,698 (GRCm39) |
missense |
probably benign |
0.28 |
BB001:Fat2
|
UTSW |
11 |
55,153,613 (GRCm39) |
missense |
probably benign |
0.03 |
BB011:Fat2
|
UTSW |
11 |
55,153,613 (GRCm39) |
missense |
probably benign |
0.03 |
P0040:Fat2
|
UTSW |
11 |
55,173,039 (GRCm39) |
missense |
possibly damaging |
0.89 |
PIT4504001:Fat2
|
UTSW |
11 |
55,146,936 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0008:Fat2
|
UTSW |
11 |
55,202,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Fat2
|
UTSW |
11 |
55,202,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Fat2
|
UTSW |
11 |
55,153,697 (GRCm39) |
missense |
probably benign |
0.16 |
R0012:Fat2
|
UTSW |
11 |
55,153,697 (GRCm39) |
missense |
probably benign |
0.16 |
R0048:Fat2
|
UTSW |
11 |
55,200,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0048:Fat2
|
UTSW |
11 |
55,200,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0098:Fat2
|
UTSW |
11 |
55,189,431 (GRCm39) |
missense |
probably damaging |
0.98 |
R0124:Fat2
|
UTSW |
11 |
55,174,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R0127:Fat2
|
UTSW |
11 |
55,180,112 (GRCm39) |
missense |
probably benign |
0.01 |
R0130:Fat2
|
UTSW |
11 |
55,142,944 (GRCm39) |
missense |
probably benign |
0.26 |
R0131:Fat2
|
UTSW |
11 |
55,164,037 (GRCm39) |
missense |
probably benign |
|
R0158:Fat2
|
UTSW |
11 |
55,187,011 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:Fat2
|
UTSW |
11 |
55,187,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Fat2
|
UTSW |
11 |
55,182,919 (GRCm39) |
splice site |
probably benign |
|
R0384:Fat2
|
UTSW |
11 |
55,160,291 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0390:Fat2
|
UTSW |
11 |
55,201,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R0403:Fat2
|
UTSW |
11 |
55,161,175 (GRCm39) |
missense |
probably benign |
0.42 |
R0416:Fat2
|
UTSW |
11 |
55,174,960 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0437:Fat2
|
UTSW |
11 |
55,173,625 (GRCm39) |
missense |
probably benign |
0.02 |
R0463:Fat2
|
UTSW |
11 |
55,153,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0497:Fat2
|
UTSW |
11 |
55,174,228 (GRCm39) |
missense |
probably benign |
0.03 |
R0617:Fat2
|
UTSW |
11 |
55,202,669 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0622:Fat2
|
UTSW |
11 |
55,173,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Fat2
|
UTSW |
11 |
55,200,035 (GRCm39) |
missense |
probably damaging |
0.97 |
R0811:Fat2
|
UTSW |
11 |
55,144,459 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0812:Fat2
|
UTSW |
11 |
55,144,459 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0869:Fat2
|
UTSW |
11 |
55,202,601 (GRCm39) |
missense |
probably benign |
0.08 |
R0870:Fat2
|
UTSW |
11 |
55,202,601 (GRCm39) |
missense |
probably benign |
0.08 |
R0899:Fat2
|
UTSW |
11 |
55,147,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R1278:Fat2
|
UTSW |
11 |
55,159,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:Fat2
|
UTSW |
11 |
55,201,599 (GRCm39) |
missense |
probably benign |
|
R1428:Fat2
|
UTSW |
11 |
55,186,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1438:Fat2
|
UTSW |
11 |
55,178,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Fat2
|
UTSW |
11 |
55,153,499 (GRCm39) |
missense |
probably benign |
|
R1506:Fat2
|
UTSW |
11 |
55,175,090 (GRCm39) |
missense |
probably benign |
|
R1547:Fat2
|
UTSW |
11 |
55,143,081 (GRCm39) |
missense |
probably benign |
0.01 |
R1554:Fat2
|
UTSW |
11 |
55,144,490 (GRCm39) |
missense |
probably benign |
0.01 |
R1562:Fat2
|
UTSW |
11 |
55,200,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Fat2
|
UTSW |
11 |
55,174,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Fat2
|
UTSW |
11 |
55,182,696 (GRCm39) |
splice site |
probably null |
|
R1601:Fat2
|
UTSW |
11 |
55,172,836 (GRCm39) |
missense |
probably benign |
0.01 |
R1610:Fat2
|
UTSW |
11 |
55,169,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Fat2
|
UTSW |
11 |
55,175,545 (GRCm39) |
missense |
probably benign |
|
R1634:Fat2
|
UTSW |
11 |
55,158,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1644:Fat2
|
UTSW |
11 |
55,187,007 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1644:Fat2
|
UTSW |
11 |
55,178,609 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1691:Fat2
|
UTSW |
11 |
55,202,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R1734:Fat2
|
UTSW |
11 |
55,172,197 (GRCm39) |
missense |
probably benign |
0.00 |
R1748:Fat2
|
UTSW |
11 |
55,147,473 (GRCm39) |
missense |
probably damaging |
0.97 |
R1771:Fat2
|
UTSW |
11 |
55,201,691 (GRCm39) |
missense |
probably benign |
0.01 |
R1800:Fat2
|
UTSW |
11 |
55,174,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1807:Fat2
|
UTSW |
11 |
55,180,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Fat2
|
UTSW |
11 |
55,147,606 (GRCm39) |
missense |
probably benign |
0.29 |
R1848:Fat2
|
UTSW |
11 |
55,202,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Fat2
|
UTSW |
11 |
55,182,840 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Fat2
|
UTSW |
11 |
55,153,004 (GRCm39) |
missense |
probably benign |
|
R1954:Fat2
|
UTSW |
11 |
55,201,910 (GRCm39) |
missense |
probably benign |
0.06 |
R2010:Fat2
|
UTSW |
11 |
55,144,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R2011:Fat2
|
UTSW |
11 |
55,173,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Fat2
|
UTSW |
11 |
55,172,686 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2081:Fat2
|
UTSW |
11 |
55,200,503 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2106:Fat2
|
UTSW |
11 |
55,147,390 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Fat2
|
UTSW |
11 |
55,194,542 (GRCm39) |
missense |
probably benign |
0.00 |
R2176:Fat2
|
UTSW |
11 |
55,158,401 (GRCm39) |
critical splice donor site |
probably null |
|
R2284:Fat2
|
UTSW |
11 |
55,173,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R2338:Fat2
|
UTSW |
11 |
55,202,727 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2340:Fat2
|
UTSW |
11 |
55,160,922 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2427:Fat2
|
UTSW |
11 |
55,201,638 (GRCm39) |
missense |
probably benign |
0.15 |
R2444:Fat2
|
UTSW |
11 |
55,172,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R2858:Fat2
|
UTSW |
11 |
55,174,599 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2882:Fat2
|
UTSW |
11 |
55,202,131 (GRCm39) |
missense |
probably damaging |
0.96 |
R3029:Fat2
|
UTSW |
11 |
55,175,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R3085:Fat2
|
UTSW |
11 |
55,142,997 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3121:Fat2
|
UTSW |
11 |
55,202,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Fat2
|
UTSW |
11 |
55,169,824 (GRCm39) |
missense |
probably benign |
0.01 |
R3500:Fat2
|
UTSW |
11 |
55,151,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R3607:Fat2
|
UTSW |
11 |
55,172,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R3611:Fat2
|
UTSW |
11 |
55,202,895 (GRCm39) |
missense |
probably benign |
|
R3620:Fat2
|
UTSW |
11 |
55,147,521 (GRCm39) |
missense |
probably damaging |
0.97 |
R3688:Fat2
|
UTSW |
11 |
55,171,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R3704:Fat2
|
UTSW |
11 |
55,200,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Fat2
|
UTSW |
11 |
55,147,012 (GRCm39) |
missense |
probably benign |
|
R3889:Fat2
|
UTSW |
11 |
55,172,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R3951:Fat2
|
UTSW |
11 |
55,187,208 (GRCm39) |
missense |
probably benign |
0.00 |
R4211:Fat2
|
UTSW |
11 |
55,174,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Fat2
|
UTSW |
11 |
55,175,127 (GRCm39) |
missense |
probably damaging |
0.98 |
R4406:Fat2
|
UTSW |
11 |
55,153,094 (GRCm39) |
missense |
probably benign |
0.00 |
R4433:Fat2
|
UTSW |
11 |
55,200,466 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4436:Fat2
|
UTSW |
11 |
55,187,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R4498:Fat2
|
UTSW |
11 |
55,160,923 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4560:Fat2
|
UTSW |
11 |
55,156,777 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4594:Fat2
|
UTSW |
11 |
55,175,578 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4663:Fat2
|
UTSW |
11 |
55,187,039 (GRCm39) |
nonsense |
probably null |
|
R4669:Fat2
|
UTSW |
11 |
55,202,441 (GRCm39) |
missense |
probably benign |
0.01 |
R4696:Fat2
|
UTSW |
11 |
55,175,841 (GRCm39) |
missense |
probably benign |
0.00 |
R4734:Fat2
|
UTSW |
11 |
55,202,294 (GRCm39) |
missense |
probably benign |
0.01 |
R4749:Fat2
|
UTSW |
11 |
55,202,294 (GRCm39) |
missense |
probably benign |
0.01 |
R4765:Fat2
|
UTSW |
11 |
55,172,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Fat2
|
UTSW |
11 |
55,175,886 (GRCm39) |
missense |
probably benign |
0.03 |
R4805:Fat2
|
UTSW |
11 |
55,174,805 (GRCm39) |
missense |
probably benign |
0.01 |
R4822:Fat2
|
UTSW |
11 |
55,202,144 (GRCm39) |
missense |
probably benign |
0.02 |
R4840:Fat2
|
UTSW |
11 |
55,169,844 (GRCm39) |
missense |
probably benign |
0.21 |
R4849:Fat2
|
UTSW |
11 |
55,201,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Fat2
|
UTSW |
11 |
55,169,859 (GRCm39) |
missense |
probably benign |
0.00 |
R4993:Fat2
|
UTSW |
11 |
55,173,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R5097:Fat2
|
UTSW |
11 |
55,201,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R5104:Fat2
|
UTSW |
11 |
55,169,814 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5115:Fat2
|
UTSW |
11 |
55,187,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Fat2
|
UTSW |
11 |
55,144,658 (GRCm39) |
missense |
probably benign |
0.00 |
R5254:Fat2
|
UTSW |
11 |
55,172,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Fat2
|
UTSW |
11 |
55,178,704 (GRCm39) |
missense |
probably benign |
0.00 |
R5288:Fat2
|
UTSW |
11 |
55,158,482 (GRCm39) |
missense |
probably benign |
0.00 |
R5355:Fat2
|
UTSW |
11 |
55,172,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Fat2
|
UTSW |
11 |
55,153,646 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Fat2
|
UTSW |
11 |
55,194,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R5411:Fat2
|
UTSW |
11 |
55,143,052 (GRCm39) |
missense |
probably benign |
0.23 |
R5416:Fat2
|
UTSW |
11 |
55,194,514 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5480:Fat2
|
UTSW |
11 |
55,200,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R5486:Fat2
|
UTSW |
11 |
55,144,507 (GRCm39) |
missense |
probably benign |
0.00 |
R5526:Fat2
|
UTSW |
11 |
55,160,187 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5532:Fat2
|
UTSW |
11 |
55,153,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Fat2
|
UTSW |
11 |
55,144,715 (GRCm39) |
missense |
probably benign |
0.00 |
R5588:Fat2
|
UTSW |
11 |
55,173,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R5598:Fat2
|
UTSW |
11 |
55,171,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Fat2
|
UTSW |
11 |
55,173,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5653:Fat2
|
UTSW |
11 |
55,201,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R5657:Fat2
|
UTSW |
11 |
55,201,507 (GRCm39) |
nonsense |
probably null |
|
R5660:Fat2
|
UTSW |
11 |
55,175,002 (GRCm39) |
missense |
probably benign |
0.00 |
R5752:Fat2
|
UTSW |
11 |
55,180,063 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5757:Fat2
|
UTSW |
11 |
55,143,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5792:Fat2
|
UTSW |
11 |
55,153,151 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5872:Fat2
|
UTSW |
11 |
55,161,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Fat2
|
UTSW |
11 |
55,174,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Fat2
|
UTSW |
11 |
55,201,129 (GRCm39) |
nonsense |
probably null |
|
R6030:Fat2
|
UTSW |
11 |
55,201,129 (GRCm39) |
nonsense |
probably null |
|
R6032:Fat2
|
UTSW |
11 |
55,144,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Fat2
|
UTSW |
11 |
55,144,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Fat2
|
UTSW |
11 |
55,186,898 (GRCm39) |
critical splice donor site |
probably null |
|
R6253:Fat2
|
UTSW |
11 |
55,187,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Fat2
|
UTSW |
11 |
55,153,407 (GRCm39) |
missense |
probably benign |
|
R6307:Fat2
|
UTSW |
11 |
55,172,106 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6450:Fat2
|
UTSW |
11 |
55,180,136 (GRCm39) |
missense |
probably damaging |
0.97 |
R6453:Fat2
|
UTSW |
11 |
55,173,042 (GRCm39) |
missense |
probably benign |
0.29 |
R6455:Fat2
|
UTSW |
11 |
55,161,283 (GRCm39) |
missense |
probably damaging |
0.96 |
R6483:Fat2
|
UTSW |
11 |
55,187,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6504:Fat2
|
UTSW |
11 |
55,153,223 (GRCm39) |
missense |
probably benign |
0.00 |
R6520:Fat2
|
UTSW |
11 |
55,175,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R6525:Fat2
|
UTSW |
11 |
55,174,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6617:Fat2
|
UTSW |
11 |
55,186,931 (GRCm39) |
missense |
probably benign |
0.01 |
R6652:Fat2
|
UTSW |
11 |
55,143,088 (GRCm39) |
missense |
probably benign |
|
R6679:Fat2
|
UTSW |
11 |
55,200,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R6680:Fat2
|
UTSW |
11 |
55,201,684 (GRCm39) |
nonsense |
probably null |
|
R6762:Fat2
|
UTSW |
11 |
55,144,308 (GRCm39) |
splice site |
probably null |
|
R6810:Fat2
|
UTSW |
11 |
55,173,067 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6818:Fat2
|
UTSW |
11 |
55,200,167 (GRCm39) |
missense |
probably benign |
0.31 |
R6919:Fat2
|
UTSW |
11 |
55,173,597 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6939:Fat2
|
UTSW |
11 |
55,143,300 (GRCm39) |
nonsense |
probably null |
|
R6941:Fat2
|
UTSW |
11 |
55,152,914 (GRCm39) |
missense |
probably benign |
|
R7023:Fat2
|
UTSW |
11 |
55,201,328 (GRCm39) |
missense |
probably benign |
0.00 |
R7027:Fat2
|
UTSW |
11 |
55,160,259 (GRCm39) |
missense |
probably benign |
0.03 |
R7027:Fat2
|
UTSW |
11 |
55,172,677 (GRCm39) |
nonsense |
probably null |
|
R7095:Fat2
|
UTSW |
11 |
55,202,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Fat2
|
UTSW |
11 |
55,174,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Fat2
|
UTSW |
11 |
55,173,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Fat2
|
UTSW |
11 |
55,172,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167:Fat2
|
UTSW |
11 |
55,175,827 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7213:Fat2
|
UTSW |
11 |
55,171,871 (GRCm39) |
nonsense |
probably null |
|
R7246:Fat2
|
UTSW |
11 |
55,187,208 (GRCm39) |
missense |
probably benign |
0.00 |
R7252:Fat2
|
UTSW |
11 |
55,202,088 (GRCm39) |
missense |
probably damaging |
0.98 |
R7266:Fat2
|
UTSW |
11 |
55,175,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R7316:Fat2
|
UTSW |
11 |
55,176,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Fat2
|
UTSW |
11 |
55,173,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R7355:Fat2
|
UTSW |
11 |
55,147,377 (GRCm39) |
missense |
probably benign |
0.00 |
R7431:Fat2
|
UTSW |
11 |
55,199,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7459:Fat2
|
UTSW |
11 |
55,194,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7460:Fat2
|
UTSW |
11 |
55,169,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Fat2
|
UTSW |
11 |
55,201,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Fat2
|
UTSW |
11 |
55,194,479 (GRCm39) |
missense |
probably benign |
0.31 |
R7678:Fat2
|
UTSW |
11 |
55,173,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R7689:Fat2
|
UTSW |
11 |
55,200,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R7704:Fat2
|
UTSW |
11 |
55,175,173 (GRCm39) |
missense |
probably benign |
0.03 |
R7710:Fat2
|
UTSW |
11 |
55,201,589 (GRCm39) |
missense |
probably benign |
0.35 |
R7724:Fat2
|
UTSW |
11 |
55,175,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7731:Fat2
|
UTSW |
11 |
55,201,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7739:Fat2
|
UTSW |
11 |
55,171,957 (GRCm39) |
nonsense |
probably null |
|
R7757:Fat2
|
UTSW |
11 |
55,202,247 (GRCm39) |
missense |
probably benign |
0.00 |
R7876:Fat2
|
UTSW |
11 |
55,202,046 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Fat2
|
UTSW |
11 |
55,144,190 (GRCm39) |
splice site |
probably null |
|
R7924:Fat2
|
UTSW |
11 |
55,153,613 (GRCm39) |
missense |
probably benign |
0.03 |
R7936:Fat2
|
UTSW |
11 |
55,201,986 (GRCm39) |
nonsense |
probably null |
|
R7936:Fat2
|
UTSW |
11 |
55,200,993 (GRCm39) |
missense |
probably benign |
|
R7938:Fat2
|
UTSW |
11 |
55,163,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7947:Fat2
|
UTSW |
11 |
55,178,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R8049:Fat2
|
UTSW |
11 |
55,202,892 (GRCm39) |
missense |
probably benign |
0.13 |
R8094:Fat2
|
UTSW |
11 |
55,186,965 (GRCm39) |
missense |
probably benign |
0.06 |
R8157:Fat2
|
UTSW |
11 |
55,142,910 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8170:Fat2
|
UTSW |
11 |
55,161,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R8172:Fat2
|
UTSW |
11 |
55,178,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8182:Fat2
|
UTSW |
11 |
55,175,223 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8188:Fat2
|
UTSW |
11 |
55,163,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R8204:Fat2
|
UTSW |
11 |
55,175,436 (GRCm39) |
missense |
probably benign |
0.02 |
R8211:Fat2
|
UTSW |
11 |
55,203,035 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8255:Fat2
|
UTSW |
11 |
55,161,101 (GRCm39) |
missense |
probably benign |
0.19 |
R8263:Fat2
|
UTSW |
11 |
55,174,962 (GRCm39) |
missense |
probably benign |
|
R8269:Fat2
|
UTSW |
11 |
55,173,535 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8443:Fat2
|
UTSW |
11 |
55,202,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Fat2
|
UTSW |
11 |
55,147,530 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8480:Fat2
|
UTSW |
11 |
55,173,794 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8511:Fat2
|
UTSW |
11 |
55,200,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R8680:Fat2
|
UTSW |
11 |
55,144,692 (GRCm39) |
missense |
probably benign |
|
R8704:Fat2
|
UTSW |
11 |
55,172,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8711:Fat2
|
UTSW |
11 |
55,159,129 (GRCm39) |
missense |
probably benign |
0.22 |
R8724:Fat2
|
UTSW |
11 |
55,173,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R8788:Fat2
|
UTSW |
11 |
55,171,929 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8802:Fat2
|
UTSW |
11 |
55,173,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8902:Fat2
|
UTSW |
11 |
55,200,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Fat2
|
UTSW |
11 |
55,147,636 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8956:Fat2
|
UTSW |
11 |
55,173,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Fat2
|
UTSW |
11 |
55,194,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R9100:Fat2
|
UTSW |
11 |
55,153,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9132:Fat2
|
UTSW |
11 |
55,189,436 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9173:Fat2
|
UTSW |
11 |
55,169,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R9241:Fat2
|
UTSW |
11 |
55,147,566 (GRCm39) |
missense |
probably benign |
0.00 |
R9253:Fat2
|
UTSW |
11 |
55,201,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9280:Fat2
|
UTSW |
11 |
55,201,523 (GRCm39) |
missense |
probably benign |
0.36 |
R9351:Fat2
|
UTSW |
11 |
55,172,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Fat2
|
UTSW |
11 |
55,201,514 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9404:Fat2
|
UTSW |
11 |
55,144,348 (GRCm39) |
critical splice donor site |
probably null |
|
R9431:Fat2
|
UTSW |
11 |
55,142,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Fat2
|
UTSW |
11 |
55,200,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R9509:Fat2
|
UTSW |
11 |
55,200,713 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9514:Fat2
|
UTSW |
11 |
55,175,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R9606:Fat2
|
UTSW |
11 |
55,180,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Fat2
|
UTSW |
11 |
55,147,605 (GRCm39) |
missense |
probably benign |
0.29 |
R9727:Fat2
|
UTSW |
11 |
55,159,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Fat2
|
UTSW |
11 |
55,194,751 (GRCm39) |
missense |
probably damaging |
1.00 |
X0010:Fat2
|
UTSW |
11 |
55,143,086 (GRCm39) |
missense |
probably benign |
0.00 |
X0011:Fat2
|
UTSW |
11 |
55,201,257 (GRCm39) |
missense |
probably damaging |
0.98 |
X0018:Fat2
|
UTSW |
11 |
55,187,036 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Fat2
|
UTSW |
11 |
55,200,240 (GRCm39) |
missense |
possibly damaging |
0.84 |
X0067:Fat2
|
UTSW |
11 |
55,174,060 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Fat2
|
UTSW |
11 |
55,175,817 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat2
|
UTSW |
11 |
55,173,621 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat2
|
UTSW |
11 |
55,200,947 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Fat2
|
UTSW |
11 |
55,194,526 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fat2
|
UTSW |
11 |
55,169,792 (GRCm39) |
nonsense |
probably null |
|
Z1186:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1186:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1187:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1188:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1188:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1189:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1189:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1190:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1190:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1191:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1191:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1192:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1192:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
|