Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
G |
A |
14: 35,532,024 (GRCm39) |
Q184* |
probably null |
Het |
A1bg |
A |
C |
15: 60,789,742 (GRCm39) |
I502S |
possibly damaging |
Het |
Actl11 |
T |
C |
9: 107,805,775 (GRCm39) |
S33P |
probably benign |
Het |
Aftph |
G |
T |
11: 20,659,632 (GRCm39) |
D730E |
probably damaging |
Het |
Arhgap29 |
A |
G |
3: 121,767,773 (GRCm39) |
|
probably benign |
Het |
Brf1 |
T |
G |
12: 112,924,795 (GRCm39) |
E643A |
probably benign |
Het |
Caskin1 |
G |
T |
17: 24,722,914 (GRCm39) |
|
probably null |
Het |
Ccnjl |
T |
C |
11: 43,476,154 (GRCm39) |
V259A |
probably benign |
Het |
Ccser2 |
G |
T |
14: 36,662,920 (GRCm39) |
T88K |
probably benign |
Het |
Cdk17 |
T |
C |
10: 93,074,824 (GRCm39) |
|
probably benign |
Het |
Clec16a |
G |
A |
16: 10,395,774 (GRCm39) |
S309N |
possibly damaging |
Het |
Cpxm1 |
C |
A |
2: 130,233,191 (GRCm39) |
A633S |
probably benign |
Het |
Ctnnbl1 |
A |
T |
2: 157,661,468 (GRCm39) |
N326I |
probably damaging |
Het |
Cyp46a1 |
T |
C |
12: 108,318,234 (GRCm39) |
V215A |
possibly damaging |
Het |
Daxx |
A |
G |
17: 34,132,454 (GRCm39) |
D528G |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,121,701 (GRCm39) |
Y1427C |
probably damaging |
Het |
Dpy19l3 |
G |
A |
7: 35,422,169 (GRCm39) |
T228I |
probably damaging |
Het |
Fam131c |
C |
T |
4: 141,109,761 (GRCm39) |
A131V |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,482,592 (GRCm39) |
T3061A |
possibly damaging |
Het |
Fgl2 |
T |
A |
5: 21,578,175 (GRCm39) |
L154H |
possibly damaging |
Het |
Fhod3 |
T |
A |
18: 25,155,924 (GRCm39) |
I514K |
probably benign |
Het |
Ficd |
G |
A |
5: 113,876,622 (GRCm39) |
G266S |
probably damaging |
Het |
Frem3 |
A |
G |
8: 81,340,544 (GRCm39) |
T946A |
probably benign |
Het |
Gan |
T |
A |
8: 117,913,917 (GRCm39) |
V105D |
probably damaging |
Het |
Garin5b |
A |
G |
7: 4,761,722 (GRCm39) |
V330A |
probably benign |
Het |
Gramd1c |
A |
G |
16: 43,811,061 (GRCm39) |
V221A |
probably damaging |
Het |
Hacd1 |
A |
G |
2: 14,040,667 (GRCm39) |
V196A |
probably benign |
Het |
Kcna6 |
C |
A |
6: 126,715,576 (GRCm39) |
V438L |
probably damaging |
Het |
Klhl41 |
T |
C |
2: 69,508,582 (GRCm39) |
V512A |
probably benign |
Het |
Lrfn1 |
A |
G |
7: 28,166,111 (GRCm39) |
T502A |
probably damaging |
Het |
Notch3 |
A |
T |
17: 32,377,844 (GRCm39) |
F105I |
possibly damaging |
Het |
Or4b13 |
T |
G |
2: 90,082,953 (GRCm39) |
K126N |
probably damaging |
Het |
Or5m10 |
A |
T |
2: 85,717,306 (GRCm39) |
H54L |
probably benign |
Het |
P3h1 |
C |
T |
4: 119,092,480 (GRCm39) |
T171I |
probably damaging |
Het |
Pcdhb1 |
A |
G |
18: 37,399,366 (GRCm39) |
E439G |
possibly damaging |
Het |
Pik3c3 |
A |
T |
18: 30,423,578 (GRCm39) |
K225* |
probably null |
Het |
Pik3c3 |
A |
G |
18: 30,426,102 (GRCm39) |
|
probably benign |
Het |
Pik3r5 |
T |
A |
11: 68,377,452 (GRCm39) |
|
probably null |
Het |
Pnpt1 |
A |
C |
11: 29,098,272 (GRCm39) |
|
probably benign |
Het |
Ppp2r1b |
T |
A |
9: 50,789,422 (GRCm39) |
V495D |
probably damaging |
Het |
Rbfox3 |
C |
A |
11: 118,396,440 (GRCm39) |
|
probably benign |
Het |
Sec14l2 |
G |
A |
11: 4,053,966 (GRCm39) |
P234S |
possibly damaging |
Het |
Sec16a |
A |
C |
2: 26,328,915 (GRCm39) |
D1033E |
probably benign |
Het |
Septin14 |
A |
G |
5: 129,763,019 (GRCm39) |
V357A |
probably damaging |
Het |
Sf3a3 |
C |
T |
4: 124,612,136 (GRCm39) |
T131I |
possibly damaging |
Het |
Snrpa |
A |
T |
7: 26,892,395 (GRCm39) |
M55K |
probably benign |
Het |
Swt1 |
G |
T |
1: 151,286,760 (GRCm39) |
T244N |
probably benign |
Het |
Tbl1xr1 |
A |
G |
3: 22,246,238 (GRCm39) |
T253A |
probably benign |
Het |
Tst |
G |
T |
15: 78,283,964 (GRCm39) |
R288S |
probably benign |
Het |
Vmn2r60 |
A |
G |
7: 41,785,910 (GRCm39) |
I238V |
probably benign |
Het |
Zbtb14 |
A |
G |
17: 69,695,184 (GRCm39) |
K294R |
probably benign |
Het |
Zfp710 |
T |
A |
7: 79,730,871 (GRCm39) |
V16E |
probably damaging |
Het |
Zfpm2 |
A |
G |
15: 40,965,320 (GRCm39) |
T602A |
probably benign |
Het |
Zfr2 |
G |
A |
10: 81,087,193 (GRCm39) |
M850I |
probably benign |
Het |
|
Other mutations in Kif14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00159:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00160:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00164:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00310:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00330:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00335:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00434:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00468:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01330:Kif14
|
APN |
1 |
136,404,112 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01530:Kif14
|
APN |
1 |
136,406,157 (GRCm39) |
splice site |
probably benign |
|
IGL01689:Kif14
|
APN |
1 |
136,447,380 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02115:Kif14
|
APN |
1 |
136,424,305 (GRCm39) |
splice site |
probably benign |
|
IGL02252:Kif14
|
APN |
1 |
136,406,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02259:Kif14
|
APN |
1 |
136,427,840 (GRCm39) |
missense |
probably benign |
|
IGL02439:Kif14
|
APN |
1 |
136,417,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Kif14
|
APN |
1 |
136,423,742 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02606:Kif14
|
APN |
1 |
136,424,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03253:Kif14
|
APN |
1 |
136,415,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0106:Kif14
|
UTSW |
1 |
136,407,662 (GRCm39) |
splice site |
probably benign |
|
R0193:Kif14
|
UTSW |
1 |
136,396,176 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0238:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0239:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0239:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0329:Kif14
|
UTSW |
1 |
136,423,764 (GRCm39) |
splice site |
probably benign |
|
R0346:Kif14
|
UTSW |
1 |
136,395,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Kif14
|
UTSW |
1 |
136,410,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Kif14
|
UTSW |
1 |
136,396,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R0590:Kif14
|
UTSW |
1 |
136,410,210 (GRCm39) |
missense |
probably damaging |
0.97 |
R0633:Kif14
|
UTSW |
1 |
136,455,043 (GRCm39) |
missense |
probably damaging |
0.96 |
R0657:Kif14
|
UTSW |
1 |
136,396,840 (GRCm39) |
missense |
probably benign |
0.07 |
R0831:Kif14
|
UTSW |
1 |
136,453,609 (GRCm39) |
splice site |
probably benign |
|
R0971:Kif14
|
UTSW |
1 |
136,447,392 (GRCm39) |
missense |
probably damaging |
0.98 |
R1018:Kif14
|
UTSW |
1 |
136,423,579 (GRCm39) |
splice site |
probably benign |
|
R1520:Kif14
|
UTSW |
1 |
136,431,062 (GRCm39) |
missense |
probably benign |
0.00 |
R1713:Kif14
|
UTSW |
1 |
136,455,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1728:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1728:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1728:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1728:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1728:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1729:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1729:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1729:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1729:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1730:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1730:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1730:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1730:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1730:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1739:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1739:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1739:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1739:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1739:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1762:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1762:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1762:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1762:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1762:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1783:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1783:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1783:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1783:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1783:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1784:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1784:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1784:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1784:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1784:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1785:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1785:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1785:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1785:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1785:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1872:Kif14
|
UTSW |
1 |
136,414,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Kif14
|
UTSW |
1 |
136,414,818 (GRCm39) |
missense |
probably benign |
|
R2049:Kif14
|
UTSW |
1 |
136,437,905 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2268:Kif14
|
UTSW |
1 |
136,447,486 (GRCm39) |
nonsense |
probably null |
|
R2373:Kif14
|
UTSW |
1 |
136,407,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R3076:Kif14
|
UTSW |
1 |
136,447,383 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3077:Kif14
|
UTSW |
1 |
136,447,383 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3078:Kif14
|
UTSW |
1 |
136,447,383 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4232:Kif14
|
UTSW |
1 |
136,444,101 (GRCm39) |
nonsense |
probably null |
|
R4246:Kif14
|
UTSW |
1 |
136,401,126 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4247:Kif14
|
UTSW |
1 |
136,401,126 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4250:Kif14
|
UTSW |
1 |
136,401,126 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4672:Kif14
|
UTSW |
1 |
136,449,016 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Kif14
|
UTSW |
1 |
136,449,017 (GRCm39) |
missense |
probably benign |
|
R4890:Kif14
|
UTSW |
1 |
136,414,868 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4994:Kif14
|
UTSW |
1 |
136,410,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5102:Kif14
|
UTSW |
1 |
136,444,141 (GRCm39) |
missense |
probably benign |
0.00 |
R5185:Kif14
|
UTSW |
1 |
136,455,207 (GRCm39) |
nonsense |
probably null |
|
R5201:Kif14
|
UTSW |
1 |
136,431,145 (GRCm39) |
missense |
probably benign |
0.00 |
R5399:Kif14
|
UTSW |
1 |
136,431,062 (GRCm39) |
missense |
probably benign |
0.00 |
R5431:Kif14
|
UTSW |
1 |
136,424,433 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5932:Kif14
|
UTSW |
1 |
136,444,128 (GRCm39) |
missense |
probably benign |
0.23 |
R6027:Kif14
|
UTSW |
1 |
136,410,797 (GRCm39) |
splice site |
probably null |
|
R6246:Kif14
|
UTSW |
1 |
136,404,162 (GRCm39) |
nonsense |
probably null |
|
R6331:Kif14
|
UTSW |
1 |
136,443,724 (GRCm39) |
missense |
probably null |
1.00 |
R6448:Kif14
|
UTSW |
1 |
136,431,085 (GRCm39) |
missense |
probably damaging |
0.99 |
R6453:Kif14
|
UTSW |
1 |
136,410,042 (GRCm39) |
splice site |
probably null |
|
R6475:Kif14
|
UTSW |
1 |
136,455,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Kif14
|
UTSW |
1 |
136,443,697 (GRCm39) |
missense |
probably benign |
0.39 |
R6713:Kif14
|
UTSW |
1 |
136,453,544 (GRCm39) |
missense |
probably benign |
|
R7173:Kif14
|
UTSW |
1 |
136,406,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R7174:Kif14
|
UTSW |
1 |
136,448,995 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7241:Kif14
|
UTSW |
1 |
136,396,491 (GRCm39) |
missense |
probably benign |
0.41 |
R7674:Kif14
|
UTSW |
1 |
136,396,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R7688:Kif14
|
UTSW |
1 |
136,422,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Kif14
|
UTSW |
1 |
136,399,191 (GRCm39) |
missense |
probably benign |
0.10 |
R7722:Kif14
|
UTSW |
1 |
136,396,033 (GRCm39) |
missense |
probably benign |
0.00 |
R7763:Kif14
|
UTSW |
1 |
136,444,121 (GRCm39) |
missense |
probably benign |
0.00 |
R7882:Kif14
|
UTSW |
1 |
136,443,763 (GRCm39) |
missense |
probably benign |
0.43 |
R7882:Kif14
|
UTSW |
1 |
136,399,314 (GRCm39) |
critical splice donor site |
probably null |
|
R8077:Kif14
|
UTSW |
1 |
136,399,186 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8101:Kif14
|
UTSW |
1 |
136,404,090 (GRCm39) |
missense |
probably benign |
0.14 |
R8308:Kif14
|
UTSW |
1 |
136,443,651 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8338:Kif14
|
UTSW |
1 |
136,422,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R8527:Kif14
|
UTSW |
1 |
136,396,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8542:Kif14
|
UTSW |
1 |
136,396,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8884:Kif14
|
UTSW |
1 |
136,414,089 (GRCm39) |
missense |
|
|
R9435:Kif14
|
UTSW |
1 |
136,401,174 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9499:Kif14
|
UTSW |
1 |
136,455,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R9551:Kif14
|
UTSW |
1 |
136,455,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R9577:Kif14
|
UTSW |
1 |
136,399,138 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Kif14
|
UTSW |
1 |
136,418,014 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kif14
|
UTSW |
1 |
136,427,754 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Kif14
|
UTSW |
1 |
136,424,391 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
|
|