Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
T |
G |
7: 12,246,507 (GRCm39) |
M1R |
probably null |
Het |
4933440N22Rik |
C |
A |
6: 117,884,540 (GRCm39) |
|
probably benign |
Het |
5031439G07Rik |
G |
T |
15: 84,837,345 (GRCm39) |
P280T |
probably damaging |
Het |
Abca2 |
C |
T |
2: 25,331,308 (GRCm39) |
S1267L |
probably damaging |
Het |
Acsl3 |
A |
T |
1: 78,684,126 (GRCm39) |
R719S |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,839 (GRCm39) |
|
probably null |
Het |
Adamts7 |
T |
C |
9: 90,070,851 (GRCm39) |
|
probably benign |
Het |
Adgrf3 |
G |
A |
5: 30,407,227 (GRCm39) |
|
probably benign |
Het |
Aldh6a1 |
T |
C |
12: 84,488,544 (GRCm39) |
E89G |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,525,752 (GRCm39) |
Y238C |
probably damaging |
Het |
Ankrd65 |
G |
A |
4: 155,877,362 (GRCm39) |
R291Q |
probably benign |
Het |
Ano2 |
C |
T |
6: 125,773,227 (GRCm39) |
R287W |
probably damaging |
Het |
Ap1ar |
A |
G |
3: 127,606,215 (GRCm39) |
I125T |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,293,197 (GRCm39) |
D705G |
probably damaging |
Het |
Asb18 |
T |
A |
1: 89,924,005 (GRCm39) |
N86I |
probably damaging |
Het |
Bicral |
A |
T |
17: 47,135,519 (GRCm39) |
S564T |
probably benign |
Het |
Bpifa6 |
A |
G |
2: 153,831,192 (GRCm39) |
M253V |
probably benign |
Het |
Braf |
T |
C |
6: 39,642,017 (GRCm39) |
D194G |
probably damaging |
Het |
Brinp3 |
C |
A |
1: 146,777,700 (GRCm39) |
P716T |
probably benign |
Het |
C7 |
T |
A |
15: 5,041,631 (GRCm39) |
Y425F |
probably damaging |
Het |
Ccdc102a |
T |
C |
8: 95,632,714 (GRCm39) |
K421R |
probably benign |
Het |
Cep89 |
G |
A |
7: 35,120,388 (GRCm39) |
|
probably null |
Het |
Chgb |
A |
T |
2: 132,634,720 (GRCm39) |
M221L |
probably benign |
Het |
Chst14 |
A |
G |
2: 118,758,145 (GRCm39) |
Y313C |
probably damaging |
Het |
Ciita |
G |
A |
16: 10,331,152 (GRCm39) |
|
probably null |
Het |
Clec12b |
A |
T |
6: 129,357,603 (GRCm39) |
I85N |
probably damaging |
Het |
Clec2e |
G |
T |
6: 129,070,459 (GRCm39) |
Y187* |
probably null |
Het |
Crbn |
T |
C |
6: 106,767,804 (GRCm39) |
K229E |
probably benign |
Het |
Ctdspl2 |
A |
T |
2: 121,811,762 (GRCm39) |
Q201L |
probably benign |
Het |
Ctrb1 |
G |
T |
8: 112,416,041 (GRCm39) |
|
probably benign |
Het |
Cyp2c55 |
T |
A |
19: 38,999,525 (GRCm39) |
V77E |
probably damaging |
Het |
Cyp2c69 |
A |
C |
19: 39,837,839 (GRCm39) |
D414E |
probably damaging |
Het |
Ddx47 |
T |
C |
6: 134,988,703 (GRCm39) |
|
probably benign |
Het |
Dlg1 |
A |
G |
16: 31,661,640 (GRCm39) |
|
probably null |
Het |
Dnah5 |
C |
A |
15: 28,230,609 (GRCm39) |
S169* |
probably null |
Het |
Dock4 |
C |
A |
12: 40,805,809 (GRCm39) |
T927K |
probably benign |
Het |
Esrp2 |
T |
G |
8: 106,860,453 (GRCm39) |
D259A |
probably damaging |
Het |
Fam169a |
A |
G |
13: 97,255,038 (GRCm39) |
K418R |
probably benign |
Het |
Fancm |
A |
T |
12: 65,146,067 (GRCm39) |
I597F |
probably damaging |
Het |
Fastkd2 |
G |
T |
1: 63,771,385 (GRCm39) |
|
probably benign |
Het |
Fbxw10 |
A |
T |
11: 62,753,464 (GRCm39) |
D486V |
probably damaging |
Het |
Fech |
C |
T |
18: 64,603,744 (GRCm39) |
|
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,766,942 (GRCm39) |
E342K |
probably benign |
Het |
Foxp1 |
T |
A |
6: 98,955,181 (GRCm39) |
H195L |
possibly damaging |
Het |
Gfra1 |
T |
A |
19: 58,440,407 (GRCm39) |
I138L |
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,806,501 (GRCm39) |
D230G |
possibly damaging |
Het |
Gm14403 |
T |
A |
2: 177,199,024 (GRCm39) |
|
probably benign |
Het |
Gpd2 |
A |
C |
2: 57,245,786 (GRCm39) |
T439P |
probably damaging |
Het |
Gpm6a |
A |
T |
8: 55,490,385 (GRCm39) |
K20N |
probably damaging |
Het |
Hc |
A |
T |
2: 34,873,819 (GRCm39) |
Y158* |
probably null |
Het |
Hectd4 |
A |
T |
5: 121,487,235 (GRCm39) |
D3410V |
possibly damaging |
Het |
Il17b |
G |
A |
18: 61,823,483 (GRCm39) |
|
probably null |
Het |
Irx4 |
G |
T |
13: 73,413,695 (GRCm39) |
R55L |
possibly damaging |
Het |
Itgav |
A |
T |
2: 83,596,245 (GRCm39) |
|
probably benign |
Het |
Lama3 |
T |
C |
18: 12,574,164 (GRCm39) |
V582A |
probably benign |
Het |
Ldhd |
G |
T |
8: 112,353,925 (GRCm39) |
A425E |
possibly damaging |
Het |
Lrp1b |
C |
T |
2: 40,817,841 (GRCm39) |
|
probably null |
Het |
Lrp5 |
T |
C |
19: 3,670,191 (GRCm39) |
T638A |
possibly damaging |
Het |
Lrrk1 |
A |
C |
7: 65,909,722 (GRCm39) |
F1996C |
probably damaging |
Het |
Ly6h |
G |
A |
15: 75,437,986 (GRCm39) |
S21L |
probably benign |
Het |
Mctp1 |
T |
C |
13: 76,973,392 (GRCm39) |
V431A |
probably benign |
Het |
Metap2 |
C |
T |
10: 93,707,345 (GRCm39) |
|
probably null |
Het |
Mfsd2b |
T |
A |
12: 4,920,536 (GRCm39) |
K94* |
probably null |
Het |
Micall2 |
A |
G |
5: 139,705,097 (GRCm39) |
L79P |
probably damaging |
Het |
Mucl2 |
T |
C |
15: 103,927,673 (GRCm39) |
T95A |
possibly damaging |
Het |
Myo15a |
A |
T |
11: 60,396,832 (GRCm39) |
T2634S |
probably damaging |
Het |
Myo5b |
G |
T |
18: 74,873,574 (GRCm39) |
V1467L |
probably damaging |
Het |
Nfic |
G |
T |
10: 81,256,414 (GRCm39) |
D105E |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,873,865 (GRCm39) |
F227Y |
probably benign |
Het |
Nrp2 |
A |
T |
1: 62,777,458 (GRCm39) |
I88F |
probably damaging |
Het |
Nup160 |
A |
T |
2: 90,530,887 (GRCm39) |
H515L |
probably benign |
Het |
Nup205 |
G |
A |
6: 35,202,917 (GRCm39) |
|
probably null |
Het |
Oas1g |
G |
A |
5: 121,020,069 (GRCm39) |
T179I |
probably benign |
Het |
Ogfr |
A |
T |
2: 180,236,543 (GRCm39) |
E376V |
probably damaging |
Het |
Or2l13 |
T |
G |
16: 19,306,378 (GRCm39) |
S263R |
probably benign |
Het |
Or4a69 |
A |
T |
2: 89,312,855 (GRCm39) |
V208D |
possibly damaging |
Het |
Or4c107 |
T |
G |
2: 88,789,387 (GRCm39) |
Y192* |
probably null |
Het |
Or52d1 |
G |
T |
7: 103,755,896 (GRCm39) |
V137F |
possibly damaging |
Het |
Or5p6 |
C |
T |
7: 107,631,595 (GRCm39) |
|
probably null |
Het |
Pard3b |
T |
C |
1: 62,384,188 (GRCm39) |
V851A |
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,611,142 (GRCm39) |
Y34F |
probably damaging |
Het |
Pikfyve |
T |
C |
1: 65,290,825 (GRCm39) |
Y1215H |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,593,565 (GRCm39) |
V1516E |
probably damaging |
Het |
Pla2g4a |
A |
T |
1: 149,763,344 (GRCm39) |
|
probably benign |
Het |
Ptprg |
A |
T |
14: 12,190,767 (GRCm38) |
I818F |
probably benign |
Het |
Ralgapb |
A |
G |
2: 158,304,173 (GRCm39) |
E644G |
possibly damaging |
Het |
Rbm45 |
A |
G |
2: 76,202,459 (GRCm39) |
I127M |
probably damaging |
Het |
Rtp2 |
T |
C |
16: 23,746,220 (GRCm39) |
Y157C |
probably damaging |
Het |
Sema3f |
A |
T |
9: 107,564,771 (GRCm39) |
|
probably benign |
Het |
Sf3b3 |
A |
T |
8: 111,564,006 (GRCm39) |
Y329N |
probably damaging |
Het |
Sfxn1 |
A |
G |
13: 54,239,646 (GRCm39) |
|
probably null |
Het |
Shkbp1 |
A |
T |
7: 27,044,751 (GRCm39) |
C447S |
probably damaging |
Het |
Sipa1l3 |
A |
G |
7: 29,021,685 (GRCm39) |
S689P |
possibly damaging |
Het |
Slc7a8 |
A |
G |
14: 54,970,656 (GRCm39) |
S332P |
probably damaging |
Het |
Slit1 |
C |
A |
19: 41,596,823 (GRCm39) |
C1092F |
probably damaging |
Het |
Slx9 |
A |
G |
10: 77,333,360 (GRCm39) |
|
probably benign |
Het |
Stard9 |
A |
G |
2: 120,533,678 (GRCm39) |
I619V |
possibly damaging |
Het |
Sycp3 |
T |
C |
10: 88,305,454 (GRCm39) |
V185A |
possibly damaging |
Het |
Taar9 |
A |
T |
10: 23,985,382 (GRCm39) |
N17K |
possibly damaging |
Het |
Tbkbp1 |
T |
C |
11: 97,039,814 (GRCm39) |
E102G |
probably damaging |
Het |
Tex44 |
A |
G |
1: 86,354,834 (GRCm39) |
N248D |
probably benign |
Het |
Tmem63b |
C |
G |
17: 45,989,904 (GRCm39) |
R88P |
possibly damaging |
Het |
Tnpo1 |
C |
T |
13: 98,986,665 (GRCm39) |
V781I |
probably benign |
Het |
Tonsl |
C |
T |
15: 76,520,761 (GRCm39) |
|
probably null |
Het |
Ttc6 |
A |
G |
12: 57,721,463 (GRCm39) |
K984R |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,391,171 (GRCm39) |
E2263G |
probably damaging |
Het |
Usp8 |
A |
G |
2: 126,596,847 (GRCm39) |
K875E |
probably damaging |
Het |
Vapb |
C |
T |
2: 173,603,905 (GRCm39) |
|
probably benign |
Het |
Vmn1r223 |
A |
G |
13: 23,434,038 (GRCm39) |
I211V |
possibly damaging |
Het |
Vmn2r81 |
G |
A |
10: 79,129,496 (GRCm39) |
V796I |
probably damaging |
Het |
Wdr90 |
A |
T |
17: 26,073,027 (GRCm39) |
V856D |
probably damaging |
Het |
Wnk2 |
T |
A |
13: 49,235,571 (GRCm39) |
T615S |
probably damaging |
Het |
|
Other mutations in Fat1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Fat1
|
APN |
8 |
45,477,639 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00157:Fat1
|
APN |
8 |
45,404,707 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL00481:Fat1
|
APN |
8 |
45,503,977 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00983:Fat1
|
APN |
8 |
45,486,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01089:Fat1
|
APN |
8 |
45,470,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01135:Fat1
|
APN |
8 |
45,477,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01143:Fat1
|
APN |
8 |
45,488,569 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01155:Fat1
|
APN |
8 |
45,476,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01376:Fat1
|
APN |
8 |
45,479,878 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01411:Fat1
|
APN |
8 |
45,479,837 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01443:Fat1
|
APN |
8 |
45,493,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01453:Fat1
|
APN |
8 |
45,504,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01606:Fat1
|
APN |
8 |
45,476,086 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01622:Fat1
|
APN |
8 |
45,482,592 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01623:Fat1
|
APN |
8 |
45,482,592 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01672:Fat1
|
APN |
8 |
45,493,737 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01735:Fat1
|
APN |
8 |
45,489,276 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01793:Fat1
|
APN |
8 |
45,442,149 (GRCm39) |
missense |
probably benign |
|
IGL01820:Fat1
|
APN |
8 |
45,463,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01969:Fat1
|
APN |
8 |
45,405,636 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02012:Fat1
|
APN |
8 |
45,480,577 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02227:Fat1
|
APN |
8 |
45,476,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02256:Fat1
|
APN |
8 |
45,403,369 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02273:Fat1
|
APN |
8 |
45,403,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02317:Fat1
|
APN |
8 |
45,478,855 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02324:Fat1
|
APN |
8 |
45,493,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Fat1
|
APN |
8 |
45,404,620 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02442:Fat1
|
APN |
8 |
45,403,360 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02486:Fat1
|
APN |
8 |
45,478,109 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02551:Fat1
|
APN |
8 |
45,504,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02617:Fat1
|
APN |
8 |
45,488,628 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02698:Fat1
|
APN |
8 |
45,476,201 (GRCm39) |
missense |
probably benign |
|
IGL02885:Fat1
|
APN |
8 |
45,442,204 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02904:Fat1
|
APN |
8 |
45,493,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02953:Fat1
|
APN |
8 |
45,477,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Fat1
|
APN |
8 |
45,476,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03153:Fat1
|
APN |
8 |
45,483,160 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03183:Fat1
|
APN |
8 |
45,403,623 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03327:Fat1
|
APN |
8 |
45,403,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03405:Fat1
|
APN |
8 |
45,478,278 (GRCm39) |
missense |
probably damaging |
1.00 |
Laggardly
|
UTSW |
8 |
45,497,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257_fat1_465
|
UTSW |
8 |
45,403,408 (GRCm39) |
missense |
probably damaging |
1.00 |
Shrinkage
|
UTSW |
8 |
45,471,074 (GRCm39) |
missense |
probably damaging |
1.00 |
F5493:Fat1
|
UTSW |
8 |
45,478,517 (GRCm39) |
missense |
probably damaging |
0.99 |
G1citation:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
I2289:Fat1
|
UTSW |
8 |
45,478,033 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02837:Fat1
|
UTSW |
8 |
45,470,471 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4283001:Fat1
|
UTSW |
8 |
45,490,244 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Fat1
|
UTSW |
8 |
45,482,577 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4576001:Fat1
|
UTSW |
8 |
45,477,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0078:Fat1
|
UTSW |
8 |
45,406,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Fat1
|
UTSW |
8 |
45,479,590 (GRCm39) |
missense |
probably benign |
0.00 |
R0328:Fat1
|
UTSW |
8 |
45,476,827 (GRCm39) |
missense |
probably benign |
0.35 |
R0367:Fat1
|
UTSW |
8 |
45,477,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Fat1
|
UTSW |
8 |
45,404,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Fat1
|
UTSW |
8 |
45,463,160 (GRCm39) |
missense |
probably damaging |
0.97 |
R0389:Fat1
|
UTSW |
8 |
45,403,385 (GRCm39) |
missense |
probably benign |
0.00 |
R0433:Fat1
|
UTSW |
8 |
45,477,686 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0456:Fat1
|
UTSW |
8 |
45,482,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Fat1
|
UTSW |
8 |
45,403,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Fat1
|
UTSW |
8 |
45,475,988 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Fat1
|
UTSW |
8 |
45,404,369 (GRCm39) |
nonsense |
probably null |
|
R0624:Fat1
|
UTSW |
8 |
45,504,205 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0701:Fat1
|
UTSW |
8 |
45,479,590 (GRCm39) |
missense |
probably benign |
0.00 |
R0723:Fat1
|
UTSW |
8 |
45,479,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Fat1
|
UTSW |
8 |
45,493,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0788:Fat1
|
UTSW |
8 |
45,477,020 (GRCm39) |
missense |
probably benign |
0.27 |
R0862:Fat1
|
UTSW |
8 |
45,471,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:Fat1
|
UTSW |
8 |
45,471,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R0907:Fat1
|
UTSW |
8 |
45,479,635 (GRCm39) |
missense |
probably benign |
0.08 |
R0962:Fat1
|
UTSW |
8 |
45,486,363 (GRCm39) |
splice site |
probably benign |
|
R1051:Fat1
|
UTSW |
8 |
45,497,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1156:Fat1
|
UTSW |
8 |
45,492,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1237:Fat1
|
UTSW |
8 |
45,497,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Fat1
|
UTSW |
8 |
45,463,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Fat1
|
UTSW |
8 |
45,478,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R1482:Fat1
|
UTSW |
8 |
45,406,281 (GRCm39) |
missense |
probably benign |
0.04 |
R1496:Fat1
|
UTSW |
8 |
45,486,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R1498:Fat1
|
UTSW |
8 |
45,478,521 (GRCm39) |
nonsense |
probably null |
|
R1508:Fat1
|
UTSW |
8 |
45,479,899 (GRCm39) |
missense |
probably benign |
0.01 |
R1577:Fat1
|
UTSW |
8 |
45,476,420 (GRCm39) |
missense |
probably benign |
0.30 |
R1646:Fat1
|
UTSW |
8 |
45,471,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Fat1
|
UTSW |
8 |
45,478,215 (GRCm39) |
nonsense |
probably null |
|
R1656:Fat1
|
UTSW |
8 |
45,478,567 (GRCm39) |
nonsense |
probably null |
|
R1662:Fat1
|
UTSW |
8 |
45,406,201 (GRCm39) |
missense |
probably benign |
0.20 |
R1672:Fat1
|
UTSW |
8 |
45,489,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1704:Fat1
|
UTSW |
8 |
45,478,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1708:Fat1
|
UTSW |
8 |
45,477,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Fat1
|
UTSW |
8 |
45,463,519 (GRCm39) |
missense |
probably benign |
0.00 |
R1812:Fat1
|
UTSW |
8 |
45,489,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Fat1
|
UTSW |
8 |
45,491,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Fat1
|
UTSW |
8 |
45,406,341 (GRCm39) |
missense |
probably benign |
0.01 |
R1883:Fat1
|
UTSW |
8 |
45,504,184 (GRCm39) |
missense |
probably benign |
0.17 |
R1893:Fat1
|
UTSW |
8 |
45,476,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1930:Fat1
|
UTSW |
8 |
45,497,265 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1931:Fat1
|
UTSW |
8 |
45,497,265 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1952:Fat1
|
UTSW |
8 |
45,486,963 (GRCm39) |
missense |
probably benign |
0.00 |
R1957:Fat1
|
UTSW |
8 |
45,493,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Fat1
|
UTSW |
8 |
45,405,430 (GRCm39) |
missense |
probably damaging |
0.96 |
R2019:Fat1
|
UTSW |
8 |
45,476,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Fat1
|
UTSW |
8 |
45,477,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Fat1
|
UTSW |
8 |
45,479,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Fat1
|
UTSW |
8 |
45,490,500 (GRCm39) |
missense |
probably benign |
0.33 |
R2196:Fat1
|
UTSW |
8 |
45,477,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Fat1
|
UTSW |
8 |
45,476,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Fat1
|
UTSW |
8 |
45,403,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Fat1
|
UTSW |
8 |
45,403,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Fat1
|
UTSW |
8 |
45,493,567 (GRCm39) |
splice site |
probably benign |
|
R2416:Fat1
|
UTSW |
8 |
45,479,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3021:Fat1
|
UTSW |
8 |
45,497,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R3108:Fat1
|
UTSW |
8 |
45,498,210 (GRCm39) |
splice site |
probably null |
|
R3109:Fat1
|
UTSW |
8 |
45,498,210 (GRCm39) |
splice site |
probably null |
|
R3196:Fat1
|
UTSW |
8 |
45,404,905 (GRCm39) |
missense |
probably benign |
0.00 |
R3683:Fat1
|
UTSW |
8 |
45,470,975 (GRCm39) |
missense |
probably benign |
|
R3732:Fat1
|
UTSW |
8 |
45,406,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3732:Fat1
|
UTSW |
8 |
45,406,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3733:Fat1
|
UTSW |
8 |
45,406,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3753:Fat1
|
UTSW |
8 |
45,478,516 (GRCm39) |
missense |
probably damaging |
0.97 |
R3905:Fat1
|
UTSW |
8 |
45,476,072 (GRCm39) |
missense |
probably benign |
0.00 |
R3907:Fat1
|
UTSW |
8 |
45,476,072 (GRCm39) |
missense |
probably benign |
0.00 |
R3908:Fat1
|
UTSW |
8 |
45,476,072 (GRCm39) |
missense |
probably benign |
0.00 |
R4060:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4061:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4062:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4063:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4078:Fat1
|
UTSW |
8 |
45,442,159 (GRCm39) |
missense |
probably damaging |
0.99 |
R4105:Fat1
|
UTSW |
8 |
45,489,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Fat1
|
UTSW |
8 |
45,503,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Fat1
|
UTSW |
8 |
45,463,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Fat1
|
UTSW |
8 |
45,489,824 (GRCm39) |
missense |
probably benign |
0.00 |
R4364:Fat1
|
UTSW |
8 |
45,405,999 (GRCm39) |
missense |
probably benign |
0.01 |
R4394:Fat1
|
UTSW |
8 |
45,405,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4395:Fat1
|
UTSW |
8 |
45,405,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4396:Fat1
|
UTSW |
8 |
45,405,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4412:Fat1
|
UTSW |
8 |
45,476,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R4542:Fat1
|
UTSW |
8 |
45,494,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Fat1
|
UTSW |
8 |
45,479,279 (GRCm39) |
missense |
probably benign |
|
R4606:Fat1
|
UTSW |
8 |
45,403,720 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4612:Fat1
|
UTSW |
8 |
45,478,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Fat1
|
UTSW |
8 |
45,486,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Fat1
|
UTSW |
8 |
45,491,363 (GRCm39) |
missense |
probably benign |
0.04 |
R4824:Fat1
|
UTSW |
8 |
45,442,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Fat1
|
UTSW |
8 |
45,489,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Fat1
|
UTSW |
8 |
45,466,102 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4849:Fat1
|
UTSW |
8 |
45,466,007 (GRCm39) |
missense |
probably benign |
0.15 |
R4896:Fat1
|
UTSW |
8 |
45,404,317 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4927:Fat1
|
UTSW |
8 |
45,476,000 (GRCm39) |
missense |
probably damaging |
0.96 |
R4941:Fat1
|
UTSW |
8 |
45,489,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5011:Fat1
|
UTSW |
8 |
45,484,300 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5040:Fat1
|
UTSW |
8 |
45,476,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Fat1
|
UTSW |
8 |
45,477,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Fat1
|
UTSW |
8 |
45,404,851 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5161:Fat1
|
UTSW |
8 |
45,405,549 (GRCm39) |
missense |
probably benign |
0.00 |
R5162:Fat1
|
UTSW |
8 |
45,478,846 (GRCm39) |
missense |
probably benign |
0.02 |
R5353:Fat1
|
UTSW |
8 |
45,489,168 (GRCm39) |
missense |
probably benign |
0.13 |
R5425:Fat1
|
UTSW |
8 |
45,478,922 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5458:Fat1
|
UTSW |
8 |
45,466,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Fat1
|
UTSW |
8 |
45,489,912 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5543:Fat1
|
UTSW |
8 |
45,476,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R5569:Fat1
|
UTSW |
8 |
45,492,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R5610:Fat1
|
UTSW |
8 |
45,406,109 (GRCm39) |
nonsense |
probably null |
|
R5734:Fat1
|
UTSW |
8 |
45,504,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R5832:Fat1
|
UTSW |
8 |
45,470,460 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5860:Fat1
|
UTSW |
8 |
45,504,166 (GRCm39) |
missense |
probably benign |
|
R5886:Fat1
|
UTSW |
8 |
45,486,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R5886:Fat1
|
UTSW |
8 |
45,480,718 (GRCm39) |
critical splice donor site |
probably null |
|
R5919:Fat1
|
UTSW |
8 |
45,479,910 (GRCm39) |
critical splice donor site |
probably null |
|
R5930:Fat1
|
UTSW |
8 |
45,497,073 (GRCm39) |
missense |
probably benign |
0.10 |
R5960:Fat1
|
UTSW |
8 |
45,486,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Fat1
|
UTSW |
8 |
45,482,493 (GRCm39) |
missense |
probably benign |
0.00 |
R6166:Fat1
|
UTSW |
8 |
45,405,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R6184:Fat1
|
UTSW |
8 |
45,406,429 (GRCm39) |
missense |
probably benign |
0.00 |
R6208:Fat1
|
UTSW |
8 |
45,480,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R6351:Fat1
|
UTSW |
8 |
45,486,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R6391:Fat1
|
UTSW |
8 |
45,405,379 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6701:Fat1
|
UTSW |
8 |
45,403,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Fat1
|
UTSW |
8 |
45,406,083 (GRCm39) |
missense |
probably benign |
0.28 |
R6703:Fat1
|
UTSW |
8 |
45,406,083 (GRCm39) |
missense |
probably benign |
0.28 |
R6704:Fat1
|
UTSW |
8 |
45,477,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R6822:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:Fat1
|
UTSW |
8 |
45,488,635 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6863:Fat1
|
UTSW |
8 |
45,497,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R6885:Fat1
|
UTSW |
8 |
45,405,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6912:Fat1
|
UTSW |
8 |
45,504,060 (GRCm39) |
missense |
probably benign |
0.00 |
R6927:Fat1
|
UTSW |
8 |
45,477,532 (GRCm39) |
missense |
probably benign |
0.41 |
R6964:Fat1
|
UTSW |
8 |
45,496,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7010:Fat1
|
UTSW |
8 |
45,406,386 (GRCm39) |
nonsense |
probably null |
|
R7062:Fat1
|
UTSW |
8 |
45,403,253 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R7063:Fat1
|
UTSW |
8 |
45,493,812 (GRCm39) |
missense |
probably benign |
0.09 |
R7071:Fat1
|
UTSW |
8 |
45,442,145 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7117:Fat1
|
UTSW |
8 |
45,484,505 (GRCm39) |
missense |
probably damaging |
0.98 |
R7146:Fat1
|
UTSW |
8 |
45,403,962 (GRCm39) |
missense |
probably benign |
|
R7210:Fat1
|
UTSW |
8 |
45,476,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R7227:Fat1
|
UTSW |
8 |
45,463,646 (GRCm39) |
missense |
probably benign |
0.08 |
R7270:Fat1
|
UTSW |
8 |
45,490,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R7373:Fat1
|
UTSW |
8 |
45,479,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7390:Fat1
|
UTSW |
8 |
45,405,511 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7465:Fat1
|
UTSW |
8 |
45,497,189 (GRCm39) |
missense |
probably benign |
0.35 |
R7476:Fat1
|
UTSW |
8 |
45,484,311 (GRCm39) |
missense |
probably benign |
0.01 |
R7483:Fat1
|
UTSW |
8 |
45,476,197 (GRCm39) |
missense |
probably benign |
0.13 |
R7484:Fat1
|
UTSW |
8 |
45,489,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Fat1
|
UTSW |
8 |
45,476,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Fat1
|
UTSW |
8 |
45,442,031 (GRCm39) |
missense |
probably benign |
0.01 |
R7554:Fat1
|
UTSW |
8 |
45,490,202 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7620:Fat1
|
UTSW |
8 |
45,462,887 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7652:Fat1
|
UTSW |
8 |
45,406,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R7694:Fat1
|
UTSW |
8 |
45,441,967 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7746:Fat1
|
UTSW |
8 |
45,404,670 (GRCm39) |
missense |
probably damaging |
0.96 |
R7762:Fat1
|
UTSW |
8 |
45,490,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R7762:Fat1
|
UTSW |
8 |
45,476,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Fat1
|
UTSW |
8 |
45,403,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R7801:Fat1
|
UTSW |
8 |
45,495,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7807:Fat1
|
UTSW |
8 |
45,495,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7821:Fat1
|
UTSW |
8 |
45,403,261 (GRCm39) |
missense |
probably benign |
|
R7869:Fat1
|
UTSW |
8 |
45,504,259 (GRCm39) |
missense |
probably benign |
0.02 |
R8034:Fat1
|
UTSW |
8 |
45,404,728 (GRCm39) |
missense |
probably benign |
0.28 |
R8094:Fat1
|
UTSW |
8 |
45,405,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R8111:Fat1
|
UTSW |
8 |
45,479,095 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8220:Fat1
|
UTSW |
8 |
45,492,993 (GRCm39) |
missense |
probably null |
|
R8221:Fat1
|
UTSW |
8 |
45,406,390 (GRCm39) |
missense |
|
|
R8233:Fat1
|
UTSW |
8 |
45,405,055 (GRCm39) |
missense |
|
|
R8250:Fat1
|
UTSW |
8 |
45,406,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R8279:Fat1
|
UTSW |
8 |
45,483,384 (GRCm39) |
critical splice donor site |
probably null |
|
R8726:Fat1
|
UTSW |
8 |
45,477,206 (GRCm39) |
missense |
probably benign |
0.23 |
R8875:Fat1
|
UTSW |
8 |
45,493,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Fat1
|
UTSW |
8 |
45,483,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Fat1
|
UTSW |
8 |
45,476,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8971:Fat1
|
UTSW |
8 |
45,495,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Fat1
|
UTSW |
8 |
45,484,332 (GRCm39) |
missense |
probably benign |
0.02 |
R9000:Fat1
|
UTSW |
8 |
45,497,587 (GRCm39) |
nonsense |
probably null |
|
R9032:Fat1
|
UTSW |
8 |
45,492,894 (GRCm39) |
missense |
probably benign |
0.01 |
R9076:Fat1
|
UTSW |
8 |
45,492,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Fat1
|
UTSW |
8 |
45,491,336 (GRCm39) |
missense |
probably benign |
0.00 |
R9083:Fat1
|
UTSW |
8 |
45,466,127 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9103:Fat1
|
UTSW |
8 |
45,404,850 (GRCm39) |
missense |
probably benign |
0.38 |
R9124:Fat1
|
UTSW |
8 |
45,478,064 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9124:Fat1
|
UTSW |
8 |
45,403,363 (GRCm39) |
missense |
probably benign |
|
R9128:Fat1
|
UTSW |
8 |
45,462,878 (GRCm39) |
missense |
probably benign |
0.14 |
R9148:Fat1
|
UTSW |
8 |
45,405,682 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9162:Fat1
|
UTSW |
8 |
45,404,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Fat1
|
UTSW |
8 |
45,404,791 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9276:Fat1
|
UTSW |
8 |
45,488,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R9303:Fat1
|
UTSW |
8 |
45,463,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Fat1
|
UTSW |
8 |
45,406,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R9392:Fat1
|
UTSW |
8 |
45,476,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Fat1
|
UTSW |
8 |
45,406,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R9712:Fat1
|
UTSW |
8 |
45,470,417 (GRCm39) |
missense |
probably benign |
0.05 |
R9756:Fat1
|
UTSW |
8 |
45,496,974 (GRCm39) |
missense |
probably damaging |
0.96 |
RF001:Fat1
|
UTSW |
8 |
45,442,003 (GRCm39) |
missense |
probably benign |
0.00 |
X0064:Fat1
|
UTSW |
8 |
45,478,771 (GRCm39) |
missense |
possibly damaging |
0.58 |
Z1088:Fat1
|
UTSW |
8 |
45,476,844 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Fat1
|
UTSW |
8 |
45,489,875 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat1
|
UTSW |
8 |
45,476,633 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Fat1
|
UTSW |
8 |
45,403,635 (GRCm39) |
missense |
probably benign |
|
|