Other mutations in this stock |
Total: 223 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447A16Rik |
G |
A |
15: 37,439,844 (GRCm39) |
|
probably benign |
Het |
Aadat |
A |
G |
8: 60,979,746 (GRCm39) |
T203A |
probably damaging |
Het |
Abca13 |
T |
A |
11: 9,199,680 (GRCm39) |
F104L |
probably benign |
Het |
Acox1 |
T |
A |
11: 116,089,109 (GRCm39) |
|
probably null |
Het |
Adam34l |
T |
C |
8: 44,078,620 (GRCm39) |
N535D |
probably damaging |
Het |
Adamts17 |
C |
T |
7: 66,799,704 (GRCm39) |
R1060* |
probably null |
Het |
Adgrg6 |
T |
C |
10: 14,315,526 (GRCm39) |
T593A |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,291,071 (GRCm39) |
P1454Q |
probably benign |
Het |
Ap2m1 |
T |
A |
16: 20,358,088 (GRCm39) |
N35K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Atr |
G |
A |
9: 95,779,634 (GRCm39) |
V1331I |
probably benign |
Het |
Bola1 |
C |
T |
3: 96,104,426 (GRCm39) |
G56D |
probably benign |
Het |
Brsk1 |
A |
G |
7: 4,707,218 (GRCm39) |
D257G |
probably damaging |
Het |
C4bp |
C |
G |
1: 130,570,725 (GRCm39) |
V284L |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,046,454 (GRCm39) |
F1761S |
probably benign |
Het |
Camsap2 |
C |
T |
1: 136,209,053 (GRCm39) |
R802Q |
probably benign |
Het |
Cbs |
G |
T |
17: 31,839,923 (GRCm39) |
A337E |
probably benign |
Het |
Ccdc186 |
A |
C |
19: 56,797,652 (GRCm39) |
H306Q |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cd55 |
C |
A |
1: 130,387,370 (GRCm39) |
A143S |
probably benign |
Het |
Cdh19 |
C |
A |
1: 110,821,114 (GRCm39) |
E541D |
probably damaging |
Het |
Cdh20 |
C |
G |
1: 109,993,465 (GRCm39) |
L307V |
possibly damaging |
Het |
Cfh |
C |
T |
1: 140,075,435 (GRCm39) |
V268I |
possibly damaging |
Het |
Cfhr2 |
A |
G |
1: 139,741,180 (GRCm39) |
M265T |
probably benign |
Het |
Cfhr2 |
A |
C |
1: 139,741,197 (GRCm39) |
N259K |
probably benign |
Het |
Chi3l1 |
C |
T |
1: 134,116,267 (GRCm39) |
A250V |
probably damaging |
Het |
Chrnb1 |
C |
A |
11: 69,676,588 (GRCm39) |
D388Y |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,276,448 (GRCm39) |
F360Y |
possibly damaging |
Het |
Clgn |
A |
G |
8: 84,149,659 (GRCm39) |
S387G |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Coil |
G |
A |
11: 88,864,802 (GRCm39) |
V10I |
probably damaging |
Het |
Col4a1 |
G |
A |
8: 11,262,712 (GRCm39) |
P1256S |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,939,554 (GRCm39) |
F597Y |
probably benign |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,880,015 (GRCm39) |
Q391L |
probably damaging |
Het |
Cspg4 |
G |
T |
9: 56,805,821 (GRCm39) |
V2211L |
probably benign |
Het |
Cxcr4 |
C |
T |
1: 128,517,014 (GRCm39) |
V216I |
probably benign |
Het |
Cyb5r1 |
C |
T |
1: 134,335,405 (GRCm39) |
R147W |
probably damaging |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,927,819 (GRCm39) |
H101R |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,880,666 (GRCm39) |
D3818V |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,960,345 (GRCm39) |
C2572Y |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Ehf |
T |
G |
2: 103,104,251 (GRCm39) |
T186P |
possibly damaging |
Het |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Etnk2 |
C |
A |
1: 133,293,325 (GRCm39) |
D89E |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,293,503 (GRCm39) |
G149W |
probably damaging |
Het |
Etnk2 |
C |
T |
1: 133,293,554 (GRCm39) |
R166* |
probably null |
Het |
Etnk2 |
G |
A |
1: 133,293,555 (GRCm39) |
R166Q |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,304,653 (GRCm39) |
V292E |
probably benign |
Het |
Fam187b |
C |
T |
7: 30,688,445 (GRCm39) |
Q268* |
probably null |
Het |
Fam72a |
C |
T |
1: 131,466,633 (GRCm39) |
T139M |
probably benign |
Het |
Fam72a |
T |
C |
1: 131,458,406 (GRCm39) |
I56T |
probably benign |
Het |
Fcamr |
A |
C |
1: 130,732,364 (GRCm39) |
N117T |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,739,317 (GRCm39) |
I206V |
probably benign |
Het |
Fcamr |
G |
A |
1: 130,740,366 (GRCm39) |
G262S |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,429 (GRCm39) |
I283V |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,740,475 (GRCm39) |
V298A |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,546 (GRCm39) |
M322V |
probably benign |
Het |
Fcamr |
C |
T |
1: 130,740,553 (GRCm39) |
P324L |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,742,334 (GRCm39) |
N574D |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,732,306 (GRCm39) |
R98G |
probably benign |
Het |
Fcmr |
T |
C |
1: 130,806,006 (GRCm39) |
S321P |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,803,711 (GRCm39) |
T172A |
probably benign |
Het |
Fut10 |
T |
A |
8: 31,691,418 (GRCm39) |
S88T |
probably benign |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gli2 |
G |
T |
1: 118,929,774 (GRCm39) |
H44Q |
probably benign |
Het |
Gli2 |
C |
T |
1: 118,795,817 (GRCm39) |
A113T |
possibly damaging |
Het |
Glrx2 |
C |
T |
1: 143,615,478 (GRCm39) |
A27V |
possibly damaging |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Gse1 |
G |
A |
8: 121,294,992 (GRCm39) |
|
probably benign |
Het |
Heatr4 |
T |
C |
12: 84,014,346 (GRCm39) |
I630M |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,439,902 (GRCm39) |
Y1134F |
possibly damaging |
Het |
Igfn1 |
G |
A |
1: 135,887,666 (GRCm39) |
P2466L |
probably damaging |
Het |
Igfn1 |
C |
T |
1: 135,899,865 (GRCm39) |
R482Q |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,898,149 (GRCm39) |
S806G |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,895,937 (GRCm39) |
A1543V |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,907,653 (GRCm39) |
A231T |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,910,213 (GRCm39) |
R124W |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,363 (GRCm39) |
E29G |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,421 (GRCm39) |
I10V |
unknown |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Ikbke |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ildr1 |
A |
T |
16: 36,528,698 (GRCm39) |
T48S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,945,526 (GRCm39) |
F749S |
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnh5 |
T |
C |
12: 75,184,465 (GRCm39) |
D86G |
probably benign |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif1b |
T |
C |
4: 149,272,179 (GRCm39) |
T1541A |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,087,859 (GRCm39) |
I983V |
possibly damaging |
Het |
Kif26a |
T |
C |
12: 112,143,219 (GRCm39) |
S1158P |
possibly damaging |
Het |
Kmt2d |
A |
G |
15: 98,763,013 (GRCm39) |
C279R |
probably damaging |
Het |
Kpna3 |
T |
A |
14: 61,605,150 (GRCm39) |
E499V |
probably benign |
Het |
Krt16 |
T |
C |
11: 100,138,533 (GRCm39) |
E205G |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
probably benign |
Het |
Lax1 |
G |
A |
1: 133,611,372 (GRCm39) |
P67S |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,716 (GRCm39) |
R342G |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
probably benign |
Het |
Lgr6 |
G |
T |
1: 134,918,373 (GRCm39) |
H263N |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,931,214 (GRCm39) |
S3N |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Mb21d2 |
A |
G |
16: 28,647,173 (GRCm39) |
V267A |
probably benign |
Het |
Mfrp |
A |
G |
9: 44,015,884 (GRCm39) |
T334A |
possibly damaging |
Het |
Morc1 |
T |
A |
16: 48,432,660 (GRCm39) |
D709E |
probably benign |
Het |
Mrgpra2b |
A |
G |
7: 47,114,627 (GRCm39) |
I35T |
probably benign |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,392,614 (GRCm39) |
C3206S |
probably damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Ndufaf7 |
A |
T |
17: 79,245,058 (GRCm39) |
K59M |
probably damaging |
Het |
Necab3 |
T |
C |
2: 154,388,795 (GRCm39) |
S208G |
probably benign |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or3a1c |
A |
G |
11: 74,046,802 (GRCm39) |
D274G |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or5m13b |
T |
A |
2: 85,754,466 (GRCm39) |
L285I |
possibly damaging |
Het |
Or8b12i |
A |
T |
9: 20,082,209 (GRCm39) |
Y219* |
probably null |
Het |
Otoa |
T |
C |
7: 120,724,662 (GRCm39) |
V447A |
probably benign |
Het |
Papss1 |
A |
G |
3: 131,311,728 (GRCm39) |
N319D |
probably benign |
Het |
Patj |
G |
A |
4: 98,320,017 (GRCm39) |
G428D |
possibly damaging |
Het |
Pcdhb3 |
G |
A |
18: 37,434,931 (GRCm39) |
G299D |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,159,404 (GRCm39) |
D432G |
probably damaging |
Het |
Pde5a |
G |
T |
3: 122,541,889 (GRCm39) |
L126F |
probably damaging |
Het |
Pigr |
C |
T |
1: 130,772,259 (GRCm39) |
A159V |
possibly damaging |
Het |
Pik3c2b |
C |
T |
1: 132,994,365 (GRCm39) |
P110S |
probably benign |
Het |
Pinx1 |
A |
G |
14: 64,115,559 (GRCm39) |
|
probably null |
Het |
Plec |
C |
A |
15: 76,061,892 (GRCm39) |
E2547* |
probably null |
Het |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prrx1 |
T |
A |
1: 163,089,536 (GRCm39) |
N97I |
probably damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,575 (GRCm39) |
V400A |
probably benign |
Het |
Ptprc |
C |
A |
1: 138,035,562 (GRCm39) |
E402D |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,561 (GRCm39) |
S405P |
probably benign |
Het |
Ptprc |
T |
G |
1: 138,027,414 (GRCm39) |
N478T |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,039,992 (GRCm39) |
K212E |
possibly damaging |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rbsn |
A |
T |
6: 92,167,000 (GRCm39) |
L548Q |
possibly damaging |
Het |
Ren1 |
C |
T |
1: 133,281,975 (GRCm39) |
T32I |
probably benign |
Het |
Ren1 |
T |
A |
1: 133,281,944 (GRCm39) |
W22R |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,287,745 (GRCm39) |
L360V |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,287,721 (GRCm39) |
N352Y |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,286,817 (GRCm39) |
E315D |
probably benign |
Het |
Ren1 |
C |
A |
1: 133,286,720 (GRCm39) |
|
probably null |
Het |
Ren1 |
A |
C |
1: 133,284,195 (GRCm39) |
K187Q |
probably benign |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
Het |
Rnpep |
G |
C |
1: 135,211,715 (GRCm39) |
A11G |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Ro60 |
C |
T |
1: 143,635,752 (GRCm39) |
V465I |
probably benign |
Het |
Ryr2 |
C |
T |
13: 11,602,308 (GRCm39) |
V4525M |
possibly damaging |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
probably benign |
Het |
Serpinb10 |
C |
T |
1: 107,466,203 (GRCm39) |
S63F |
probably damaging |
Het |
Serpinb2 |
G |
A |
1: 107,443,365 (GRCm39) |
A55T |
probably damaging |
Het |
Serpinb2 |
A |
C |
1: 107,452,273 (GRCm39) |
S284R |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,624 (GRCm39) |
T259I |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,620 (GRCm39) |
H258Y |
probably benign |
Het |
Serpinb2 |
C |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
Het |
Sis |
A |
T |
3: 72,872,978 (GRCm39) |
C53* |
probably null |
Het |
Slc13a5 |
C |
T |
11: 72,157,285 (GRCm39) |
|
probably null |
Het |
Slc26a9 |
C |
T |
1: 131,691,608 (GRCm39) |
A617V |
probably benign |
Het |
Slc26a9 |
C |
A |
1: 131,693,750 (GRCm39) |
R747S |
probably benign |
Het |
Slc9a8 |
T |
C |
2: 167,266,065 (GRCm39) |
F14S |
probably benign |
Het |
Spock3 |
T |
C |
8: 63,802,011 (GRCm39) |
L330P |
probably damaging |
Het |
Stab2 |
T |
G |
10: 86,773,903 (GRCm39) |
R809S |
probably benign |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
probably benign |
Het |
Steap3 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Tecta |
G |
A |
9: 42,303,218 (GRCm39) |
T138I |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,556,628 (GRCm39) |
T328I |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 129,595,674 (GRCm39) |
F498Y |
probably benign |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Traf7 |
A |
G |
17: 24,731,353 (GRCm39) |
F228L |
probably damaging |
Het |
Trhr |
A |
G |
15: 44,060,549 (GRCm39) |
E23G |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,577,968 (GRCm39) |
T779A |
probably benign |
Het |
Tusc2 |
A |
T |
9: 107,441,830 (GRCm39) |
I68F |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Upf2 |
A |
T |
2: 6,032,261 (GRCm39) |
S191C |
probably damaging |
Het |
Usp24 |
A |
G |
4: 106,217,618 (GRCm39) |
N447S |
possibly damaging |
Het |
Usp42 |
T |
C |
5: 143,700,381 (GRCm39) |
D1214G |
probably damaging |
Het |
Vcam1 |
T |
A |
3: 115,908,164 (GRCm39) |
I633L |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,507,086 (GRCm39) |
Y742C |
probably damaging |
Het |
Vmn2r81 |
C |
A |
10: 79,106,489 (GRCm39) |
T489K |
probably benign |
Het |
Ypel1 |
C |
G |
16: 16,907,283 (GRCm39) |
|
probably benign |
Het |
Zan |
C |
A |
5: 137,413,280 (GRCm39) |
|
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zfp616 |
A |
C |
11: 73,976,597 (GRCm39) |
K955N |
probably damaging |
Het |
Zfyve9 |
A |
C |
4: 108,575,698 (GRCm39) |
V461G |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
|
Other mutations in Fat3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Fat3
|
APN |
9 |
15,907,723 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL00962:Fat3
|
APN |
9 |
15,826,815 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00966:Fat3
|
APN |
9 |
15,910,390 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01100:Fat3
|
APN |
9 |
16,286,524 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01104:Fat3
|
APN |
9 |
16,287,024 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01104:Fat3
|
APN |
9 |
15,909,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01121:Fat3
|
APN |
9 |
15,909,697 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01407:Fat3
|
APN |
9 |
16,289,319 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01444:Fat3
|
APN |
9 |
15,910,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01634:Fat3
|
APN |
9 |
15,909,654 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01649:Fat3
|
APN |
9 |
16,288,015 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01839:Fat3
|
APN |
9 |
15,909,168 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01867:Fat3
|
APN |
9 |
16,289,197 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01894:Fat3
|
APN |
9 |
16,287,145 (GRCm39) |
missense |
probably benign |
|
IGL01913:Fat3
|
APN |
9 |
15,910,086 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02033:Fat3
|
APN |
9 |
15,826,648 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02035:Fat3
|
APN |
9 |
16,289,266 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02146:Fat3
|
APN |
9 |
15,910,878 (GRCm39) |
missense |
probably benign |
|
IGL02147:Fat3
|
APN |
9 |
15,907,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Fat3
|
APN |
9 |
15,908,346 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02161:Fat3
|
APN |
9 |
15,908,347 (GRCm39) |
nonsense |
probably null |
|
IGL02164:Fat3
|
APN |
9 |
15,942,720 (GRCm39) |
splice site |
probably benign |
|
IGL02269:Fat3
|
APN |
9 |
15,826,873 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02314:Fat3
|
APN |
9 |
15,881,134 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02393:Fat3
|
APN |
9 |
15,899,708 (GRCm39) |
nonsense |
probably null |
|
IGL02410:Fat3
|
APN |
9 |
15,909,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02504:Fat3
|
APN |
9 |
15,871,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02572:Fat3
|
APN |
9 |
15,871,802 (GRCm39) |
missense |
probably benign |
|
IGL02623:Fat3
|
APN |
9 |
15,908,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02654:Fat3
|
APN |
9 |
15,908,271 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02749:Fat3
|
APN |
9 |
15,918,007 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02810:Fat3
|
APN |
9 |
16,288,146 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02839:Fat3
|
APN |
9 |
15,830,466 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02890:Fat3
|
APN |
9 |
15,826,636 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02892:Fat3
|
APN |
9 |
16,288,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03090:Fat3
|
APN |
9 |
16,288,535 (GRCm39) |
nonsense |
probably null |
|
IGL03144:Fat3
|
APN |
9 |
16,286,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03199:Fat3
|
APN |
9 |
16,288,344 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03365:Fat3
|
APN |
9 |
15,907,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03392:Fat3
|
APN |
9 |
15,915,158 (GRCm39) |
missense |
probably benign |
|
IGL03408:Fat3
|
APN |
9 |
15,909,253 (GRCm39) |
nonsense |
probably null |
|
gagged
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
hushed
|
UTSW |
9 |
15,871,165 (GRCm39) |
missense |
possibly damaging |
0.72 |
Muffled
|
UTSW |
9 |
15,849,287 (GRCm39) |
critical splice donor site |
probably null |
|
muted
|
UTSW |
9 |
15,908,773 (GRCm39) |
missense |
possibly damaging |
0.93 |
Softened
|
UTSW |
9 |
16,289,481 (GRCm39) |
missense |
probably benign |
|
BB001:Fat3
|
UTSW |
9 |
15,910,593 (GRCm39) |
missense |
probably damaging |
1.00 |
BB002:Fat3
|
UTSW |
9 |
15,942,656 (GRCm39) |
missense |
possibly damaging |
0.77 |
BB011:Fat3
|
UTSW |
9 |
15,910,593 (GRCm39) |
missense |
probably damaging |
1.00 |
BB012:Fat3
|
UTSW |
9 |
15,942,656 (GRCm39) |
missense |
possibly damaging |
0.77 |
F6893:Fat3
|
UTSW |
9 |
15,918,085 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03050:Fat3
|
UTSW |
9 |
15,907,896 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4142001:Fat3
|
UTSW |
9 |
15,903,414 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4283001:Fat3
|
UTSW |
9 |
15,917,897 (GRCm39) |
missense |
possibly damaging |
0.77 |
PIT4378001:Fat3
|
UTSW |
9 |
16,288,104 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4434001:Fat3
|
UTSW |
9 |
15,907,612 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4468001:Fat3
|
UTSW |
9 |
15,907,647 (GRCm39) |
missense |
probably benign |
0.06 |
R0001:Fat3
|
UTSW |
9 |
16,289,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R0005:Fat3
|
UTSW |
9 |
15,874,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R0005:Fat3
|
UTSW |
9 |
15,874,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Fat3
|
UTSW |
9 |
15,826,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Fat3
|
UTSW |
9 |
15,877,275 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0089:Fat3
|
UTSW |
9 |
15,849,501 (GRCm39) |
missense |
probably benign |
|
R0135:Fat3
|
UTSW |
9 |
15,918,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Fat3
|
UTSW |
9 |
15,881,002 (GRCm39) |
splice site |
probably benign |
|
R0349:Fat3
|
UTSW |
9 |
15,942,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Fat3
|
UTSW |
9 |
15,909,699 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0382:Fat3
|
UTSW |
9 |
15,871,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R0418:Fat3
|
UTSW |
9 |
16,158,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R0419:Fat3
|
UTSW |
9 |
15,903,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Fat3
|
UTSW |
9 |
15,908,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Fat3
|
UTSW |
9 |
15,856,304 (GRCm39) |
splice site |
probably benign |
|
R0480:Fat3
|
UTSW |
9 |
15,909,025 (GRCm39) |
missense |
probably benign |
0.00 |
R0510:Fat3
|
UTSW |
9 |
15,910,981 (GRCm39) |
nonsense |
probably null |
|
R0665:Fat3
|
UTSW |
9 |
15,908,698 (GRCm39) |
missense |
probably benign |
|
R0715:Fat3
|
UTSW |
9 |
16,286,419 (GRCm39) |
missense |
probably benign |
|
R0727:Fat3
|
UTSW |
9 |
15,907,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0882:Fat3
|
UTSW |
9 |
15,942,664 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0946:Fat3
|
UTSW |
9 |
15,909,100 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1068:Fat3
|
UTSW |
9 |
15,881,330 (GRCm39) |
missense |
probably benign |
|
R1081:Fat3
|
UTSW |
9 |
16,286,580 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1082:Fat3
|
UTSW |
9 |
15,917,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Fat3
|
UTSW |
9 |
15,908,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Fat3
|
UTSW |
9 |
15,908,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R1233:Fat3
|
UTSW |
9 |
15,834,041 (GRCm39) |
missense |
probably benign |
|
R1306:Fat3
|
UTSW |
9 |
16,287,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R1311:Fat3
|
UTSW |
9 |
15,932,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1338:Fat3
|
UTSW |
9 |
15,836,387 (GRCm39) |
missense |
probably benign |
0.00 |
R1395:Fat3
|
UTSW |
9 |
16,158,212 (GRCm39) |
missense |
probably benign |
0.00 |
R1466:Fat3
|
UTSW |
9 |
16,286,778 (GRCm39) |
missense |
probably damaging |
0.96 |
R1466:Fat3
|
UTSW |
9 |
16,286,778 (GRCm39) |
missense |
probably damaging |
0.96 |
R1510:Fat3
|
UTSW |
9 |
15,871,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R1528:Fat3
|
UTSW |
9 |
15,836,387 (GRCm39) |
missense |
probably benign |
0.00 |
R1531:Fat3
|
UTSW |
9 |
15,908,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R1659:Fat3
|
UTSW |
9 |
15,908,479 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1697:Fat3
|
UTSW |
9 |
15,856,176 (GRCm39) |
missense |
probably benign |
0.05 |
R1699:Fat3
|
UTSW |
9 |
15,849,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Fat3
|
UTSW |
9 |
15,907,611 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1731:Fat3
|
UTSW |
9 |
15,907,233 (GRCm39) |
missense |
probably benign |
|
R1784:Fat3
|
UTSW |
9 |
15,907,611 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1789:Fat3
|
UTSW |
9 |
16,288,281 (GRCm39) |
missense |
probably benign |
0.00 |
R1794:Fat3
|
UTSW |
9 |
15,908,434 (GRCm39) |
missense |
probably benign |
0.15 |
R1794:Fat3
|
UTSW |
9 |
15,908,432 (GRCm39) |
nonsense |
probably null |
|
R1830:Fat3
|
UTSW |
9 |
15,826,636 (GRCm39) |
missense |
probably benign |
0.03 |
R1835:Fat3
|
UTSW |
9 |
15,909,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Fat3
|
UTSW |
9 |
15,878,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Fat3
|
UTSW |
9 |
15,871,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Fat3
|
UTSW |
9 |
15,909,411 (GRCm39) |
missense |
probably benign |
|
R1912:Fat3
|
UTSW |
9 |
15,881,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Fat3
|
UTSW |
9 |
15,908,353 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1967:Fat3
|
UTSW |
9 |
15,879,591 (GRCm39) |
missense |
probably benign |
0.00 |
R2070:Fat3
|
UTSW |
9 |
15,910,666 (GRCm39) |
missense |
probably benign |
0.21 |
R2100:Fat3
|
UTSW |
9 |
16,288,726 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2104:Fat3
|
UTSW |
9 |
15,909,813 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2113:Fat3
|
UTSW |
9 |
15,911,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Fat3
|
UTSW |
9 |
16,158,015 (GRCm39) |
critical splice donor site |
probably null |
|
R2136:Fat3
|
UTSW |
9 |
16,288,347 (GRCm39) |
missense |
probably benign |
0.01 |
R2146:Fat3
|
UTSW |
9 |
15,901,808 (GRCm39) |
missense |
probably benign |
0.01 |
R2233:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2234:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Fat3
|
UTSW |
9 |
15,826,558 (GRCm39) |
missense |
probably benign |
|
R2285:Fat3
|
UTSW |
9 |
16,287,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2365:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:Fat3
|
UTSW |
9 |
15,881,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R2447:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2496:Fat3
|
UTSW |
9 |
15,877,399 (GRCm39) |
missense |
probably benign |
0.01 |
R2509:Fat3
|
UTSW |
9 |
15,836,310 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2932:Fat3
|
UTSW |
9 |
16,287,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R2986:Fat3
|
UTSW |
9 |
15,903,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R3054:Fat3
|
UTSW |
9 |
15,871,792 (GRCm39) |
missense |
probably benign |
|
R3056:Fat3
|
UTSW |
9 |
15,871,792 (GRCm39) |
missense |
probably benign |
|
R3729:Fat3
|
UTSW |
9 |
16,158,337 (GRCm39) |
splice site |
probably benign |
|
R3745:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3859:Fat3
|
UTSW |
9 |
15,908,524 (GRCm39) |
nonsense |
probably null |
|
R3862:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3890:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3950:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3972:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4004:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4005:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4086:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4111:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4227:Fat3
|
UTSW |
9 |
16,288,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Fat3
|
UTSW |
9 |
16,158,074 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4394:Fat3
|
UTSW |
9 |
15,834,088 (GRCm39) |
missense |
probably benign |
0.11 |
R4403:Fat3
|
UTSW |
9 |
15,856,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R4433:Fat3
|
UTSW |
9 |
15,942,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R4453:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4479:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4480:Fat3
|
UTSW |
9 |
15,909,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4521:Fat3
|
UTSW |
9 |
15,834,238 (GRCm39) |
missense |
probably null |
0.71 |
R4620:Fat3
|
UTSW |
9 |
15,908,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Fat3
|
UTSW |
9 |
15,942,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4721:Fat3
|
UTSW |
9 |
15,941,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Fat3
|
UTSW |
9 |
15,909,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Fat3
|
UTSW |
9 |
15,911,028 (GRCm39) |
missense |
probably benign |
0.17 |
R4823:Fat3
|
UTSW |
9 |
15,907,803 (GRCm39) |
missense |
probably benign |
|
R4836:Fat3
|
UTSW |
9 |
16,289,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Fat3
|
UTSW |
9 |
15,908,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Fat3
|
UTSW |
9 |
16,289,244 (GRCm39) |
missense |
probably benign |
0.03 |
R4856:Fat3
|
UTSW |
9 |
15,932,626 (GRCm39) |
missense |
probably benign |
|
R4869:Fat3
|
UTSW |
9 |
16,288,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R4886:Fat3
|
UTSW |
9 |
15,932,626 (GRCm39) |
missense |
probably benign |
|
R4899:Fat3
|
UTSW |
9 |
15,881,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R4941:Fat3
|
UTSW |
9 |
16,286,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R4986:Fat3
|
UTSW |
9 |
15,909,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R5058:Fat3
|
UTSW |
9 |
15,908,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5079:Fat3
|
UTSW |
9 |
15,910,423 (GRCm39) |
missense |
probably benign |
0.01 |
R5080:Fat3
|
UTSW |
9 |
15,910,634 (GRCm39) |
missense |
probably benign |
0.35 |
R5174:Fat3
|
UTSW |
9 |
15,910,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Fat3
|
UTSW |
9 |
15,871,609 (GRCm39) |
missense |
probably damaging |
0.99 |
R5203:Fat3
|
UTSW |
9 |
16,289,438 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5216:Fat3
|
UTSW |
9 |
16,288,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Fat3
|
UTSW |
9 |
15,901,856 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5318:Fat3
|
UTSW |
9 |
16,287,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Fat3
|
UTSW |
9 |
16,287,739 (GRCm39) |
missense |
probably benign |
0.05 |
R5385:Fat3
|
UTSW |
9 |
15,833,971 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5436:Fat3
|
UTSW |
9 |
15,871,810 (GRCm39) |
missense |
probably benign |
0.02 |
R5437:Fat3
|
UTSW |
9 |
15,996,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R5453:Fat3
|
UTSW |
9 |
15,908,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Fat3
|
UTSW |
9 |
15,830,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R5516:Fat3
|
UTSW |
9 |
15,910,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Fat3
|
UTSW |
9 |
16,288,219 (GRCm39) |
nonsense |
probably null |
|
R5628:Fat3
|
UTSW |
9 |
15,877,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:Fat3
|
UTSW |
9 |
16,287,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5845:Fat3
|
UTSW |
9 |
16,288,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Fat3
|
UTSW |
9 |
15,849,757 (GRCm39) |
missense |
probably benign |
0.15 |
R5941:Fat3
|
UTSW |
9 |
15,910,797 (GRCm39) |
missense |
probably benign |
0.07 |
R5974:Fat3
|
UTSW |
9 |
15,917,824 (GRCm39) |
critical splice donor site |
probably null |
|
R5986:Fat3
|
UTSW |
9 |
15,909,613 (GRCm39) |
missense |
probably benign |
0.22 |
R6015:Fat3
|
UTSW |
9 |
16,287,346 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6031:Fat3
|
UTSW |
9 |
15,899,788 (GRCm39) |
missense |
probably benign |
0.02 |
R6031:Fat3
|
UTSW |
9 |
15,899,788 (GRCm39) |
missense |
probably benign |
0.02 |
R6042:Fat3
|
UTSW |
9 |
16,289,113 (GRCm39) |
missense |
probably benign |
0.12 |
R6051:Fat3
|
UTSW |
9 |
16,286,751 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6052:Fat3
|
UTSW |
9 |
15,833,975 (GRCm39) |
missense |
probably null |
|
R6119:Fat3
|
UTSW |
9 |
16,287,864 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6161:Fat3
|
UTSW |
9 |
16,288,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Fat3
|
UTSW |
9 |
15,907,441 (GRCm39) |
missense |
probably benign |
0.19 |
R6318:Fat3
|
UTSW |
9 |
15,828,280 (GRCm39) |
intron |
probably benign |
|
R6347:Fat3
|
UTSW |
9 |
15,909,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Fat3
|
UTSW |
9 |
15,849,287 (GRCm39) |
critical splice donor site |
probably null |
|
R6351:Fat3
|
UTSW |
9 |
15,849,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Fat3
|
UTSW |
9 |
15,910,466 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6460:Fat3
|
UTSW |
9 |
15,878,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Fat3
|
UTSW |
9 |
15,903,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R6533:Fat3
|
UTSW |
9 |
15,910,195 (GRCm39) |
missense |
probably benign |
0.02 |
R6565:Fat3
|
UTSW |
9 |
15,826,623 (GRCm39) |
missense |
probably benign |
|
R6576:Fat3
|
UTSW |
9 |
16,288,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R6649:Fat3
|
UTSW |
9 |
16,288,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R6716:Fat3
|
UTSW |
9 |
15,830,565 (GRCm39) |
missense |
probably benign |
|
R6719:Fat3
|
UTSW |
9 |
15,907,440 (GRCm39) |
missense |
probably benign |
|
R6753:Fat3
|
UTSW |
9 |
15,826,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6754:Fat3
|
UTSW |
9 |
15,826,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6755:Fat3
|
UTSW |
9 |
15,826,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6792:Fat3
|
UTSW |
9 |
16,286,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:Fat3
|
UTSW |
9 |
15,826,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6803:Fat3
|
UTSW |
9 |
15,908,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R6831:Fat3
|
UTSW |
9 |
16,287,847 (GRCm39) |
missense |
probably damaging |
0.98 |
R6831:Fat3
|
UTSW |
9 |
15,826,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6833:Fat3
|
UTSW |
9 |
15,826,357 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6877:Fat3
|
UTSW |
9 |
15,910,564 (GRCm39) |
missense |
probably benign |
|
R6894:Fat3
|
UTSW |
9 |
15,909,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Fat3
|
UTSW |
9 |
16,289,044 (GRCm39) |
missense |
probably benign |
0.37 |
R6931:Fat3
|
UTSW |
9 |
15,871,238 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6934:Fat3
|
UTSW |
9 |
16,288,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R6940:Fat3
|
UTSW |
9 |
15,828,096 (GRCm39) |
splice site |
probably null |
|
R6959:Fat3
|
UTSW |
9 |
15,908,181 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6969:Fat3
|
UTSW |
9 |
15,941,212 (GRCm39) |
missense |
probably benign |
0.29 |
R6986:Fat3
|
UTSW |
9 |
15,932,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Fat3
|
UTSW |
9 |
15,830,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Fat3
|
UTSW |
9 |
16,287,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Fat3
|
UTSW |
9 |
16,289,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7089:Fat3
|
UTSW |
9 |
15,908,214 (GRCm39) |
missense |
probably benign |
0.01 |
R7136:Fat3
|
UTSW |
9 |
16,289,481 (GRCm39) |
missense |
probably benign |
|
R7137:Fat3
|
UTSW |
9 |
15,908,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7154:Fat3
|
UTSW |
9 |
15,908,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Fat3
|
UTSW |
9 |
15,917,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R7183:Fat3
|
UTSW |
9 |
15,834,133 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7237:Fat3
|
UTSW |
9 |
16,288,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7288:Fat3
|
UTSW |
9 |
15,909,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Fat3
|
UTSW |
9 |
15,826,592 (GRCm39) |
missense |
|
|
R7293:Fat3
|
UTSW |
9 |
15,826,336 (GRCm39) |
missense |
|
|
R7381:Fat3
|
UTSW |
9 |
16,158,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R7438:Fat3
|
UTSW |
9 |
15,899,778 (GRCm39) |
missense |
probably benign |
|
R7537:Fat3
|
UTSW |
9 |
15,849,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Fat3
|
UTSW |
9 |
15,908,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Fat3
|
UTSW |
9 |
15,909,558 (GRCm39) |
missense |
probably benign |
0.03 |
R7623:Fat3
|
UTSW |
9 |
15,899,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R7624:Fat3
|
UTSW |
9 |
15,871,165 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7684:Fat3
|
UTSW |
9 |
15,899,564 (GRCm39) |
critical splice donor site |
probably null |
|
R7690:Fat3
|
UTSW |
9 |
15,909,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R7804:Fat3
|
UTSW |
9 |
15,901,888 (GRCm39) |
missense |
probably benign |
0.01 |
R7809:Fat3
|
UTSW |
9 |
15,917,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Fat3
|
UTSW |
9 |
15,910,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R7925:Fat3
|
UTSW |
9 |
15,942,656 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7954:Fat3
|
UTSW |
9 |
15,909,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R8021:Fat3
|
UTSW |
9 |
15,910,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R8118:Fat3
|
UTSW |
9 |
15,871,400 (GRCm39) |
missense |
probably benign |
|
R8141:Fat3
|
UTSW |
9 |
15,908,362 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8163:Fat3
|
UTSW |
9 |
15,871,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R8170:Fat3
|
UTSW |
9 |
15,858,792 (GRCm39) |
missense |
probably damaging |
0.97 |
R8201:Fat3
|
UTSW |
9 |
15,908,773 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8258:Fat3
|
UTSW |
9 |
15,901,887 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8259:Fat3
|
UTSW |
9 |
15,901,887 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8274:Fat3
|
UTSW |
9 |
16,288,786 (GRCm39) |
nonsense |
probably null |
|
R8275:Fat3
|
UTSW |
9 |
16,158,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8345:Fat3
|
UTSW |
9 |
15,910,570 (GRCm39) |
missense |
probably benign |
0.08 |
R8350:Fat3
|
UTSW |
9 |
15,826,435 (GRCm39) |
missense |
|
|
R8405:Fat3
|
UTSW |
9 |
15,907,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8421:Fat3
|
UTSW |
9 |
15,909,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R8450:Fat3
|
UTSW |
9 |
15,826,435 (GRCm39) |
missense |
|
|
R8472:Fat3
|
UTSW |
9 |
16,286,563 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8482:Fat3
|
UTSW |
9 |
16,158,263 (GRCm39) |
missense |
probably benign |
0.02 |
R8680:Fat3
|
UTSW |
9 |
15,908,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R8690:Fat3
|
UTSW |
9 |
15,878,397 (GRCm39) |
missense |
probably benign |
0.45 |
R8748:Fat3
|
UTSW |
9 |
15,834,161 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8756:Fat3
|
UTSW |
9 |
16,287,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R8834:Fat3
|
UTSW |
9 |
15,942,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:Fat3
|
UTSW |
9 |
15,878,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:Fat3
|
UTSW |
9 |
15,941,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8898:Fat3
|
UTSW |
9 |
15,858,822 (GRCm39) |
missense |
probably benign |
0.04 |
R8930:Fat3
|
UTSW |
9 |
15,910,819 (GRCm39) |
missense |
probably benign |
0.06 |
R8932:Fat3
|
UTSW |
9 |
15,910,819 (GRCm39) |
missense |
probably benign |
0.06 |
R8954:Fat3
|
UTSW |
9 |
16,287,864 (GRCm39) |
missense |
probably benign |
0.00 |
R8995:Fat3
|
UTSW |
9 |
16,286,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R9000:Fat3
|
UTSW |
9 |
15,918,095 (GRCm39) |
missense |
probably benign |
0.12 |
R9000:Fat3
|
UTSW |
9 |
15,871,816 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9060:Fat3
|
UTSW |
9 |
15,910,782 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9116:Fat3
|
UTSW |
9 |
15,909,421 (GRCm39) |
missense |
probably benign |
0.34 |
R9136:Fat3
|
UTSW |
9 |
15,833,738 (GRCm39) |
missense |
|
|
R9193:Fat3
|
UTSW |
9 |
15,910,248 (GRCm39) |
missense |
probably benign |
|
R9235:Fat3
|
UTSW |
9 |
15,833,674 (GRCm39) |
missense |
probably null |
|
R9257:Fat3
|
UTSW |
9 |
15,907,863 (GRCm39) |
missense |
probably benign |
|
R9297:Fat3
|
UTSW |
9 |
15,908,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Fat3
|
UTSW |
9 |
15,932,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R9412:Fat3
|
UTSW |
9 |
15,908,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R9427:Fat3
|
UTSW |
9 |
16,288,691 (GRCm39) |
nonsense |
probably null |
|
R9430:Fat3
|
UTSW |
9 |
16,287,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R9480:Fat3
|
UTSW |
9 |
15,942,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R9497:Fat3
|
UTSW |
9 |
15,903,504 (GRCm39) |
missense |
probably damaging |
0.99 |
R9547:Fat3
|
UTSW |
9 |
15,911,142 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9569:Fat3
|
UTSW |
9 |
15,830,495 (GRCm39) |
missense |
|
|
R9591:Fat3
|
UTSW |
9 |
16,288,336 (GRCm39) |
missense |
probably benign |
0.01 |
R9615:Fat3
|
UTSW |
9 |
16,289,343 (GRCm39) |
missense |
probably benign |
0.00 |
R9649:Fat3
|
UTSW |
9 |
15,908,054 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9671:Fat3
|
UTSW |
9 |
16,286,871 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9750:Fat3
|
UTSW |
9 |
15,915,157 (GRCm39) |
missense |
probably benign |
0.00 |
R9777:Fat3
|
UTSW |
9 |
15,826,537 (GRCm39) |
missense |
probably benign |
|
RF006:Fat3
|
UTSW |
9 |
15,909,913 (GRCm39) |
missense |
probably benign |
0.36 |
X0021:Fat3
|
UTSW |
9 |
15,941,227 (GRCm39) |
missense |
probably null |
0.66 |
X0026:Fat3
|
UTSW |
9 |
15,907,629 (GRCm39) |
missense |
probably benign |
|
X0064:Fat3
|
UTSW |
9 |
15,830,573 (GRCm39) |
missense |
probably benign |
|
Z1176:Fat3
|
UTSW |
9 |
16,286,913 (GRCm39) |
missense |
probably benign |
|
Z1176:Fat3
|
UTSW |
9 |
16,286,725 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat3
|
UTSW |
9 |
15,858,822 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Fat3
|
UTSW |
9 |
15,877,287 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1177:Fat3
|
UTSW |
9 |
15,858,834 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fat3
|
UTSW |
9 |
15,834,322 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Fat3
|
UTSW |
9 |
15,881,131 (GRCm39) |
missense |
probably damaging |
0.99 |
|