Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
T |
C |
19: 8,995,096 (GRCm39) |
V5460A |
probably benign |
Het |
Bco2 |
A |
G |
9: 50,444,755 (GRCm39) |
V517A |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,455,809 (GRCm39) |
D183E |
probably damaging |
Het |
Ccdc142 |
T |
C |
6: 83,084,941 (GRCm39) |
|
probably null |
Het |
Ccdc39 |
A |
G |
3: 33,895,327 (GRCm39) |
L34P |
probably damaging |
Het |
Cdc42bpb |
T |
A |
12: 111,302,463 (GRCm39) |
H198L |
probably damaging |
Het |
Cdc73 |
T |
A |
1: 143,485,120 (GRCm39) |
E516V |
probably damaging |
Het |
Cep170b |
T |
A |
12: 112,705,419 (GRCm39) |
L1059Q |
probably benign |
Het |
Chrm1 |
T |
C |
19: 8,655,463 (GRCm39) |
L56P |
probably damaging |
Het |
Clec4d |
T |
A |
6: 123,242,314 (GRCm39) |
V22D |
probably damaging |
Het |
Cplane1 |
T |
A |
15: 8,223,887 (GRCm39) |
N883K |
probably benign |
Het |
Cyp2c39 |
T |
C |
19: 39,549,405 (GRCm39) |
Y308H |
possibly damaging |
Het |
Cyp2d12 |
T |
C |
15: 82,441,137 (GRCm39) |
L141P |
probably damaging |
Het |
Cyp4x1 |
G |
T |
4: 114,983,791 (GRCm39) |
Q85K |
probably benign |
Het |
Dpysl5 |
G |
A |
5: 30,948,941 (GRCm39) |
D399N |
probably damaging |
Het |
Enpp7 |
T |
C |
11: 118,879,588 (GRCm39) |
|
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fitm2 |
T |
A |
2: 163,314,604 (GRCm39) |
|
probably benign |
Het |
Gng10 |
T |
A |
4: 59,035,314 (GRCm39) |
I26N |
possibly damaging |
Het |
Gpr33 |
C |
T |
12: 52,070,236 (GRCm39) |
V268I |
probably benign |
Het |
Hmcn2 |
G |
A |
2: 31,270,309 (GRCm39) |
C1182Y |
probably damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Krt36 |
C |
T |
11: 99,993,765 (GRCm39) |
V358M |
probably damaging |
Het |
Lmod3 |
T |
C |
6: 97,224,838 (GRCm39) |
I328V |
probably benign |
Het |
Lrp8 |
T |
C |
4: 107,712,987 (GRCm39) |
V580A |
probably damaging |
Het |
Masp2 |
T |
C |
4: 148,698,872 (GRCm39) |
I651T |
probably damaging |
Het |
Mnd1 |
C |
A |
3: 84,041,416 (GRCm39) |
C62F |
probably benign |
Het |
Msi2 |
A |
T |
11: 88,480,934 (GRCm39) |
S118T |
probably damaging |
Het |
Muc19 |
T |
C |
15: 91,755,747 (GRCm39) |
|
noncoding transcript |
Het |
Nabp1 |
G |
A |
1: 51,516,773 (GRCm39) |
R32* |
probably null |
Het |
Nfix |
CAAAAA |
CAAAA |
8: 85,442,876 (GRCm39) |
|
probably null |
Het |
Nup88 |
T |
C |
11: 70,856,545 (GRCm39) |
D196G |
probably damaging |
Het |
Or11h4b |
T |
C |
14: 50,919,020 (GRCm39) |
I24V |
probably benign |
Het |
Pax1 |
T |
A |
2: 147,207,722 (GRCm39) |
I198N |
probably damaging |
Het |
Pde3a |
A |
G |
6: 141,196,073 (GRCm39) |
E253G |
probably damaging |
Het |
Phldb1 |
C |
T |
9: 44,607,428 (GRCm39) |
R1192Q |
probably damaging |
Het |
Pianp |
C |
A |
6: 124,976,602 (GRCm39) |
P137Q |
probably damaging |
Het |
Prdm15 |
A |
C |
16: 97,600,464 (GRCm39) |
|
probably null |
Het |
Ptprf |
A |
T |
4: 118,126,369 (GRCm39) |
|
probably benign |
Het |
Rfx7 |
A |
G |
9: 72,525,246 (GRCm39) |
D812G |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,050,378 (GRCm39) |
T691A |
probably benign |
Het |
Rundc3a |
A |
T |
11: 102,292,914 (GRCm39) |
S436C |
probably damaging |
Het |
Sntb1 |
T |
C |
15: 55,769,714 (GRCm39) |
T92A |
possibly damaging |
Het |
Tars3 |
T |
C |
7: 65,332,596 (GRCm39) |
S566P |
probably damaging |
Het |
Tbc1d32 |
A |
T |
10: 56,026,888 (GRCm39) |
|
probably null |
Het |
Tmc2 |
C |
A |
2: 130,056,483 (GRCm39) |
|
probably null |
Het |
Tns1 |
A |
C |
1: 74,118,399 (GRCm39) |
I77S |
probably damaging |
Het |
Trpd52l3 |
T |
C |
19: 29,981,646 (GRCm39) |
W134R |
probably damaging |
Het |
Vmn2r15 |
A |
C |
5: 109,445,309 (GRCm39) |
N38K |
possibly damaging |
Het |
Wdr90 |
A |
T |
17: 26,079,362 (GRCm39) |
D257E |
probably damaging |
Het |
Zbtb9 |
T |
C |
17: 27,193,098 (GRCm39) |
C168R |
possibly damaging |
Het |
Zfp1004 |
T |
A |
2: 150,035,065 (GRCm39) |
V462E |
probably benign |
Het |
|
Other mutations in Tep1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00482:Tep1
|
APN |
14 |
51,080,641 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00490:Tep1
|
APN |
14 |
51,070,930 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01114:Tep1
|
APN |
14 |
51,088,096 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01294:Tep1
|
APN |
14 |
51,067,114 (GRCm39) |
splice site |
probably benign |
|
IGL01902:Tep1
|
APN |
14 |
51,103,548 (GRCm39) |
splice site |
probably benign |
|
IGL01910:Tep1
|
APN |
14 |
51,081,569 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01925:Tep1
|
APN |
14 |
51,061,955 (GRCm39) |
unclassified |
probably benign |
|
IGL01965:Tep1
|
APN |
14 |
51,100,952 (GRCm39) |
splice site |
probably benign |
|
IGL02071:Tep1
|
APN |
14 |
51,071,506 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02124:Tep1
|
APN |
14 |
51,091,581 (GRCm39) |
unclassified |
probably benign |
|
IGL02189:Tep1
|
APN |
14 |
51,064,283 (GRCm39) |
missense |
probably benign |
|
IGL02252:Tep1
|
APN |
14 |
51,067,712 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02299:Tep1
|
APN |
14 |
51,078,128 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02343:Tep1
|
APN |
14 |
51,066,704 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02423:Tep1
|
APN |
14 |
51,082,077 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02537:Tep1
|
APN |
14 |
51,073,570 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02601:Tep1
|
APN |
14 |
51,070,935 (GRCm39) |
nonsense |
probably null |
|
IGL02941:Tep1
|
APN |
14 |
51,103,494 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02990:Tep1
|
APN |
14 |
51,105,703 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03144:Tep1
|
APN |
14 |
51,081,474 (GRCm39) |
splice site |
probably benign |
|
IGL03209:Tep1
|
APN |
14 |
51,078,160 (GRCm39) |
splice site |
probably benign |
|
R0240_Tep1_347
|
UTSW |
14 |
51,100,486 (GRCm39) |
splice site |
probably benign |
|
R0972_Tep1_893
|
UTSW |
14 |
51,061,753 (GRCm39) |
unclassified |
probably benign |
|
R1686_Tep1_375
|
UTSW |
14 |
51,074,245 (GRCm39) |
missense |
probably benign |
0.12 |
R7232_Tep1_671
|
UTSW |
14 |
51,081,789 (GRCm39) |
missense |
unknown |
|
R8009_Tep1_822
|
UTSW |
14 |
51,061,687 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4305001:Tep1
|
UTSW |
14 |
51,066,684 (GRCm39) |
missense |
possibly damaging |
0.90 |
PIT4362001:Tep1
|
UTSW |
14 |
51,103,510 (GRCm39) |
missense |
probably benign |
0.23 |
R0058:Tep1
|
UTSW |
14 |
51,071,522 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0060:Tep1
|
UTSW |
14 |
51,103,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Tep1
|
UTSW |
14 |
51,089,373 (GRCm39) |
splice site |
probably null |
|
R0123:Tep1
|
UTSW |
14 |
51,067,150 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0134:Tep1
|
UTSW |
14 |
51,067,150 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0148:Tep1
|
UTSW |
14 |
51,062,246 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0240:Tep1
|
UTSW |
14 |
51,100,486 (GRCm39) |
splice site |
probably benign |
|
R0243:Tep1
|
UTSW |
14 |
51,084,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Tep1
|
UTSW |
14 |
51,074,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0432:Tep1
|
UTSW |
14 |
51,104,280 (GRCm39) |
small deletion |
probably benign |
|
R0464:Tep1
|
UTSW |
14 |
51,085,141 (GRCm39) |
missense |
probably benign |
0.00 |
R0566:Tep1
|
UTSW |
14 |
51,082,871 (GRCm39) |
critical splice donor site |
probably null |
|
R0691:Tep1
|
UTSW |
14 |
51,104,301 (GRCm39) |
nonsense |
probably null |
|
R0787:Tep1
|
UTSW |
14 |
51,066,687 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0972:Tep1
|
UTSW |
14 |
51,061,753 (GRCm39) |
unclassified |
probably benign |
|
R1263:Tep1
|
UTSW |
14 |
51,082,970 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1300:Tep1
|
UTSW |
14 |
51,064,512 (GRCm39) |
critical splice donor site |
probably null |
|
R1327:Tep1
|
UTSW |
14 |
51,090,556 (GRCm39) |
missense |
probably benign |
0.18 |
R1556:Tep1
|
UTSW |
14 |
51,090,499 (GRCm39) |
missense |
probably benign |
0.06 |
R1584:Tep1
|
UTSW |
14 |
51,103,494 (GRCm39) |
missense |
probably damaging |
0.98 |
R1607:Tep1
|
UTSW |
14 |
51,062,020 (GRCm39) |
missense |
probably null |
0.99 |
R1686:Tep1
|
UTSW |
14 |
51,074,245 (GRCm39) |
missense |
probably benign |
0.12 |
R1715:Tep1
|
UTSW |
14 |
51,092,024 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1778:Tep1
|
UTSW |
14 |
51,067,079 (GRCm39) |
intron |
probably benign |
|
R1993:Tep1
|
UTSW |
14 |
51,061,641 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2071:Tep1
|
UTSW |
14 |
51,091,739 (GRCm39) |
missense |
probably benign |
0.23 |
R2104:Tep1
|
UTSW |
14 |
51,088,037 (GRCm39) |
splice site |
probably benign |
|
R2118:Tep1
|
UTSW |
14 |
51,093,029 (GRCm39) |
splice site |
probably null |
|
R2119:Tep1
|
UTSW |
14 |
51,076,443 (GRCm39) |
missense |
probably benign |
0.13 |
R2241:Tep1
|
UTSW |
14 |
51,091,667 (GRCm39) |
missense |
probably benign |
0.01 |
R2243:Tep1
|
UTSW |
14 |
51,091,667 (GRCm39) |
missense |
probably benign |
0.01 |
R2311:Tep1
|
UTSW |
14 |
51,071,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2420:Tep1
|
UTSW |
14 |
51,071,480 (GRCm39) |
missense |
probably benign |
|
R2874:Tep1
|
UTSW |
14 |
51,088,107 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3084:Tep1
|
UTSW |
14 |
51,064,511 (GRCm39) |
critical splice donor site |
probably null |
|
R3086:Tep1
|
UTSW |
14 |
51,064,511 (GRCm39) |
critical splice donor site |
probably null |
|
R3621:Tep1
|
UTSW |
14 |
51,066,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R3815:Tep1
|
UTSW |
14 |
51,105,772 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4124:Tep1
|
UTSW |
14 |
51,081,191 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4125:Tep1
|
UTSW |
14 |
51,081,191 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4127:Tep1
|
UTSW |
14 |
51,081,191 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4134:Tep1
|
UTSW |
14 |
51,082,317 (GRCm39) |
missense |
probably benign |
|
R4152:Tep1
|
UTSW |
14 |
51,075,051 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4153:Tep1
|
UTSW |
14 |
51,075,051 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4191:Tep1
|
UTSW |
14 |
51,074,263 (GRCm39) |
missense |
probably damaging |
0.96 |
R4248:Tep1
|
UTSW |
14 |
51,100,351 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4293:Tep1
|
UTSW |
14 |
51,084,318 (GRCm39) |
missense |
probably benign |
|
R4569:Tep1
|
UTSW |
14 |
51,062,197 (GRCm39) |
missense |
probably benign |
0.01 |
R4704:Tep1
|
UTSW |
14 |
51,074,530 (GRCm39) |
missense |
probably benign |
0.06 |
R4815:Tep1
|
UTSW |
14 |
51,078,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R4978:Tep1
|
UTSW |
14 |
51,082,891 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4989:Tep1
|
UTSW |
14 |
51,076,457 (GRCm39) |
missense |
probably benign |
|
R5022:Tep1
|
UTSW |
14 |
51,066,456 (GRCm39) |
missense |
probably benign |
0.27 |
R5057:Tep1
|
UTSW |
14 |
51,066,456 (GRCm39) |
missense |
probably benign |
0.27 |
R5063:Tep1
|
UTSW |
14 |
51,088,084 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5118:Tep1
|
UTSW |
14 |
51,093,044 (GRCm39) |
splice site |
probably null |
|
R5128:Tep1
|
UTSW |
14 |
51,081,736 (GRCm39) |
makesense |
probably null |
|
R5149:Tep1
|
UTSW |
14 |
51,074,855 (GRCm39) |
nonsense |
probably null |
|
R5171:Tep1
|
UTSW |
14 |
51,062,259 (GRCm39) |
missense |
probably benign |
0.01 |
R5201:Tep1
|
UTSW |
14 |
51,105,567 (GRCm39) |
missense |
probably benign |
0.01 |
R5260:Tep1
|
UTSW |
14 |
51,076,088 (GRCm39) |
missense |
probably benign |
|
R5339:Tep1
|
UTSW |
14 |
51,082,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R5384:Tep1
|
UTSW |
14 |
51,105,774 (GRCm39) |
missense |
probably damaging |
0.98 |
R5385:Tep1
|
UTSW |
14 |
51,105,774 (GRCm39) |
missense |
probably damaging |
0.98 |
R5386:Tep1
|
UTSW |
14 |
51,105,774 (GRCm39) |
missense |
probably damaging |
0.98 |
R5594:Tep1
|
UTSW |
14 |
51,067,339 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5639:Tep1
|
UTSW |
14 |
51,091,062 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5749:Tep1
|
UTSW |
14 |
51,081,529 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5756:Tep1
|
UTSW |
14 |
51,074,836 (GRCm39) |
critical splice donor site |
probably null |
|
R6013:Tep1
|
UTSW |
14 |
51,098,505 (GRCm39) |
missense |
probably damaging |
0.97 |
R6014:Tep1
|
UTSW |
14 |
51,084,457 (GRCm39) |
missense |
probably benign |
0.12 |
R6248:Tep1
|
UTSW |
14 |
51,067,715 (GRCm39) |
missense |
probably damaging |
0.98 |
R6264:Tep1
|
UTSW |
14 |
51,082,970 (GRCm39) |
missense |
probably damaging |
0.99 |
R6363:Tep1
|
UTSW |
14 |
51,062,005 (GRCm39) |
missense |
probably benign |
0.04 |
R6381:Tep1
|
UTSW |
14 |
51,082,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R6462:Tep1
|
UTSW |
14 |
51,081,836 (GRCm39) |
missense |
probably benign |
|
R6942:Tep1
|
UTSW |
14 |
51,074,194 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6951:Tep1
|
UTSW |
14 |
51,071,370 (GRCm39) |
critical splice donor site |
probably null |
|
R6979:Tep1
|
UTSW |
14 |
51,076,094 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6999:Tep1
|
UTSW |
14 |
51,088,162 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7099:Tep1
|
UTSW |
14 |
51,081,944 (GRCm39) |
splice site |
probably null |
|
R7208:Tep1
|
UTSW |
14 |
51,062,013 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7232:Tep1
|
UTSW |
14 |
51,081,789 (GRCm39) |
missense |
unknown |
|
R7249:Tep1
|
UTSW |
14 |
51,061,732 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7325:Tep1
|
UTSW |
14 |
51,103,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R7409:Tep1
|
UTSW |
14 |
51,104,312 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7499:Tep1
|
UTSW |
14 |
51,091,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R7542:Tep1
|
UTSW |
14 |
51,099,948 (GRCm39) |
nonsense |
probably null |
|
R7806:Tep1
|
UTSW |
14 |
51,074,266 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7825:Tep1
|
UTSW |
14 |
51,081,344 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7901:Tep1
|
UTSW |
14 |
51,064,308 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7961:Tep1
|
UTSW |
14 |
51,061,687 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7993:Tep1
|
UTSW |
14 |
51,067,710 (GRCm39) |
missense |
probably benign |
0.41 |
R8009:Tep1
|
UTSW |
14 |
51,061,687 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8085:Tep1
|
UTSW |
14 |
51,066,753 (GRCm39) |
missense |
probably benign |
0.11 |
R8299:Tep1
|
UTSW |
14 |
51,105,502 (GRCm39) |
missense |
probably benign |
0.06 |
R8330:Tep1
|
UTSW |
14 |
51,085,162 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8396:Tep1
|
UTSW |
14 |
51,074,529 (GRCm39) |
missense |
probably benign |
0.23 |
R8475:Tep1
|
UTSW |
14 |
51,078,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R8695:Tep1
|
UTSW |
14 |
51,082,894 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8726:Tep1
|
UTSW |
14 |
51,085,080 (GRCm39) |
missense |
probably damaging |
0.98 |
R8812:Tep1
|
UTSW |
14 |
51,074,589 (GRCm39) |
missense |
probably damaging |
0.98 |
R9152:Tep1
|
UTSW |
14 |
51,104,162 (GRCm39) |
missense |
probably benign |
0.14 |
R9269:Tep1
|
UTSW |
14 |
51,081,766 (GRCm39) |
missense |
probably damaging |
0.98 |
R9299:Tep1
|
UTSW |
14 |
51,081,988 (GRCm39) |
splice site |
probably benign |
|
R9365:Tep1
|
UTSW |
14 |
51,064,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Tep1
|
UTSW |
14 |
51,066,429 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9408:Tep1
|
UTSW |
14 |
51,074,637 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9445:Tep1
|
UTSW |
14 |
51,082,967 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9487:Tep1
|
UTSW |
14 |
51,066,687 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9555:Tep1
|
UTSW |
14 |
51,105,888 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9597:Tep1
|
UTSW |
14 |
51,100,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R9715:Tep1
|
UTSW |
14 |
51,081,759 (GRCm39) |
missense |
|
|
R9732:Tep1
|
UTSW |
14 |
51,088,162 (GRCm39) |
missense |
probably benign |
0.33 |
R9777:Tep1
|
UTSW |
14 |
51,076,443 (GRCm39) |
nonsense |
probably null |
|
RF007:Tep1
|
UTSW |
14 |
51,098,402 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0024:Tep1
|
UTSW |
14 |
51,064,576 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0060:Tep1
|
UTSW |
14 |
51,074,221 (GRCm39) |
missense |
probably benign |
0.25 |
Z1177:Tep1
|
UTSW |
14 |
51,085,222 (GRCm39) |
missense |
probably damaging |
0.99 |
|