Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AB124611 |
C |
G |
9: 21,440,331 (GRCm39) |
Q106E |
probably benign |
Het |
Abi2 |
A |
G |
1: 60,492,888 (GRCm39) |
M387V |
probably null |
Het |
Adra2c |
A |
T |
5: 35,437,707 (GRCm39) |
N160Y |
probably damaging |
Het |
Ager |
G |
A |
17: 34,819,716 (GRCm39) |
R383H |
probably benign |
Het |
Arhgef28 |
C |
T |
13: 98,130,557 (GRCm39) |
R427H |
probably benign |
Het |
Atl1 |
T |
A |
12: 69,972,922 (GRCm39) |
S81T |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,947,470 (GRCm39) |
|
probably benign |
Het |
Cdh10 |
T |
A |
15: 19,013,487 (GRCm39) |
F696I |
possibly damaging |
Het |
Cdk2ap2 |
T |
C |
19: 4,147,429 (GRCm39) |
S2P |
unknown |
Het |
Cela1 |
G |
A |
15: 100,580,821 (GRCm39) |
T145I |
probably benign |
Het |
Celsr2 |
A |
T |
3: 108,303,443 (GRCm39) |
|
probably benign |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Col22a1 |
A |
G |
15: 71,878,503 (GRCm39) |
I218T |
probably damaging |
Het |
Copb1 |
T |
C |
7: 113,820,935 (GRCm39) |
I785V |
possibly damaging |
Het |
Dnajc16 |
A |
T |
4: 141,492,002 (GRCm39) |
V607E |
possibly damaging |
Het |
Dnali1 |
A |
T |
4: 124,957,414 (GRCm39) |
L110Q |
probably damaging |
Het |
Epn1 |
A |
G |
7: 5,096,375 (GRCm39) |
E223G |
probably benign |
Het |
Erbb3 |
A |
G |
10: 128,414,325 (GRCm39) |
L473P |
possibly damaging |
Het |
Fhip1a |
A |
G |
3: 85,568,318 (GRCm39) |
I1067T |
possibly damaging |
Het |
Gadl1 |
T |
A |
9: 115,835,569 (GRCm39) |
D332E |
probably benign |
Het |
Gm10801 |
TC |
TCGAC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Heg1 |
A |
G |
16: 33,570,863 (GRCm39) |
S1188G |
probably null |
Het |
Hipk3 |
G |
A |
2: 104,268,242 (GRCm39) |
A575V |
probably benign |
Het |
Htt |
T |
A |
5: 35,046,809 (GRCm39) |
I2375N |
possibly damaging |
Het |
Klhl24 |
A |
T |
16: 19,938,980 (GRCm39) |
K512* |
probably null |
Het |
Krtdap |
A |
T |
7: 30,488,952 (GRCm39) |
Y40F |
probably damaging |
Het |
Lhx1 |
A |
T |
11: 84,410,455 (GRCm39) |
S381T |
probably benign |
Het |
Lnpep |
G |
A |
17: 17,773,203 (GRCm39) |
P655L |
probably damaging |
Het |
Map6d1 |
A |
G |
16: 20,055,386 (GRCm39) |
V150A |
probably benign |
Het |
Marchf10 |
A |
G |
11: 105,292,802 (GRCm39) |
S202P |
possibly damaging |
Het |
Med1 |
A |
C |
11: 98,080,102 (GRCm39) |
L13R |
possibly damaging |
Het |
Mxi1 |
G |
A |
19: 53,360,126 (GRCm39) |
G283S |
probably damaging |
Het |
Myh7 |
T |
G |
14: 55,212,752 (GRCm39) |
D1431A |
probably damaging |
Het |
Myo3b |
G |
T |
2: 70,088,325 (GRCm39) |
G863W |
probably damaging |
Het |
Nat8f1 |
G |
T |
6: 85,887,907 (GRCm39) |
Q18K |
probably benign |
Het |
Ncaph |
A |
G |
2: 126,950,529 (GRCm39) |
V576A |
probably benign |
Het |
Nfkbia |
T |
G |
12: 55,539,196 (GRCm39) |
D39A |
possibly damaging |
Het |
Nrxn2 |
G |
T |
19: 6,555,057 (GRCm39) |
G1179C |
probably damaging |
Het |
Or12k8 |
A |
C |
2: 36,975,307 (GRCm39) |
V151G |
probably damaging |
Het |
P4ha1 |
A |
G |
10: 59,205,455 (GRCm39) |
D495G |
probably damaging |
Het |
Phf20 |
C |
T |
2: 156,144,843 (GRCm39) |
A817V |
probably benign |
Het |
Phlpp2 |
A |
T |
8: 110,652,431 (GRCm39) |
I592F |
probably benign |
Het |
Polq |
A |
G |
16: 36,832,280 (GRCm39) |
S7G |
unknown |
Het |
Ppfia3 |
G |
T |
7: 44,997,941 (GRCm39) |
Q729K |
probably benign |
Het |
Prmt8 |
A |
C |
6: 127,706,462 (GRCm39) |
F110V |
probably damaging |
Het |
Psca |
A |
T |
15: 74,587,868 (GRCm39) |
|
probably null |
Het |
Pus7 |
G |
T |
5: 23,980,754 (GRCm39) |
D165E |
probably benign |
Het |
Raver2 |
A |
G |
4: 100,994,942 (GRCm39) |
E555G |
probably damaging |
Het |
Rb1cc1 |
G |
A |
1: 6,315,395 (GRCm39) |
V457M |
probably damaging |
Het |
Rbp3 |
A |
G |
14: 33,676,522 (GRCm39) |
R157G |
probably benign |
Het |
Rin3 |
T |
G |
12: 102,335,857 (GRCm39) |
H589Q |
probably benign |
Het |
Scart2 |
A |
C |
7: 139,828,913 (GRCm39) |
T191P |
possibly damaging |
Het |
Sgk2 |
T |
A |
2: 162,854,890 (GRCm39) |
S334T |
probably damaging |
Het |
Sh2d4b |
T |
C |
14: 40,614,832 (GRCm39) |
M31V |
probably benign |
Het |
Slc23a3 |
G |
A |
1: 75,106,271 (GRCm39) |
T316I |
probably damaging |
Het |
Slc5a4b |
C |
A |
10: 75,910,925 (GRCm39) |
G304C |
probably damaging |
Het |
Slc7a14 |
A |
G |
3: 31,311,759 (GRCm39) |
V87A |
probably damaging |
Het |
Slitrk3 |
A |
T |
3: 72,956,164 (GRCm39) |
N869K |
probably benign |
Het |
St8sia6 |
T |
C |
2: 13,661,896 (GRCm39) |
R312G |
possibly damaging |
Het |
Strip2 |
A |
T |
6: 29,923,968 (GRCm39) |
E94V |
probably benign |
Het |
Sycp2 |
T |
C |
2: 177,990,052 (GRCm39) |
D1398G |
probably damaging |
Het |
Syne1 |
C |
A |
10: 5,143,040 (GRCm39) |
V114F |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,280,204 (GRCm39) |
K1630E |
probably benign |
Het |
Sytl2 |
A |
G |
7: 90,025,334 (GRCm39) |
N441D |
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,501,136 (GRCm39) |
C424R |
|
Het |
Tln2 |
T |
C |
9: 67,302,827 (GRCm39) |
D48G |
probably damaging |
Het |
Treml1 |
A |
G |
17: 48,673,852 (GRCm39) |
T288A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,596,113 (GRCm39) |
I20267V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,679,259 (GRCm39) |
V10821D |
unknown |
Het |
Xcl1 |
T |
A |
1: 164,763,079 (GRCm39) |
|
probably benign |
Het |
Zdhhc23 |
A |
T |
16: 43,794,227 (GRCm39) |
V149E |
probably damaging |
Het |
Zfp273 |
A |
T |
13: 67,970,387 (GRCm39) |
I12F |
possibly damaging |
Het |
Zfp874a |
A |
T |
13: 67,590,764 (GRCm39) |
C307S |
probably damaging |
Het |
|
Other mutations in Vmn2r111 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Vmn2r111
|
APN |
17 |
22,767,734 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01306:Vmn2r111
|
APN |
17 |
22,787,965 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01309:Vmn2r111
|
APN |
17 |
22,787,997 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01457:Vmn2r111
|
APN |
17 |
22,790,966 (GRCm39) |
nonsense |
probably null |
|
IGL01465:Vmn2r111
|
APN |
17 |
22,767,718 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01505:Vmn2r111
|
APN |
17 |
22,767,553 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01571:Vmn2r111
|
APN |
17 |
22,790,373 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01715:Vmn2r111
|
APN |
17 |
22,788,054 (GRCm39) |
splice site |
probably benign |
|
IGL01962:Vmn2r111
|
APN |
17 |
22,767,265 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02190:Vmn2r111
|
APN |
17 |
22,789,754 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02496:Vmn2r111
|
APN |
17 |
22,787,837 (GRCm39) |
missense |
probably benign |
|
IGL02519:Vmn2r111
|
APN |
17 |
22,767,320 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02616:Vmn2r111
|
APN |
17 |
22,790,031 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02641:Vmn2r111
|
APN |
17 |
22,792,205 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02690:Vmn2r111
|
APN |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02698:Vmn2r111
|
APN |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03017:Vmn2r111
|
APN |
17 |
22,789,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Vmn2r111
|
UTSW |
17 |
22,766,990 (GRCm39) |
missense |
probably benign |
|
R0064:Vmn2r111
|
UTSW |
17 |
22,791,053 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Vmn2r111
|
UTSW |
17 |
22,792,102 (GRCm39) |
missense |
probably benign |
0.02 |
R1439:Vmn2r111
|
UTSW |
17 |
22,790,097 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1636:Vmn2r111
|
UTSW |
17 |
22,790,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
R1648:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
R1697:Vmn2r111
|
UTSW |
17 |
22,767,041 (GRCm39) |
missense |
probably benign |
0.26 |
R1996:Vmn2r111
|
UTSW |
17 |
22,767,062 (GRCm39) |
missense |
probably benign |
0.21 |
R2040:Vmn2r111
|
UTSW |
17 |
22,767,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Vmn2r111
|
UTSW |
17 |
22,778,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Vmn2r111
|
UTSW |
17 |
22,792,085 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2357:Vmn2r111
|
UTSW |
17 |
22,778,151 (GRCm39) |
splice site |
probably benign |
|
R3700:Vmn2r111
|
UTSW |
17 |
22,790,142 (GRCm39) |
nonsense |
probably null |
|
R3782:Vmn2r111
|
UTSW |
17 |
22,790,301 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4085:Vmn2r111
|
UTSW |
17 |
22,778,096 (GRCm39) |
missense |
probably benign |
0.00 |
R4323:Vmn2r111
|
UTSW |
17 |
22,792,159 (GRCm39) |
missense |
probably benign |
0.02 |
R4900:Vmn2r111
|
UTSW |
17 |
22,767,637 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5072:Vmn2r111
|
UTSW |
17 |
22,767,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R5123:Vmn2r111
|
UTSW |
17 |
22,790,124 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5181:Vmn2r111
|
UTSW |
17 |
22,790,001 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5357:Vmn2r111
|
UTSW |
17 |
22,767,083 (GRCm39) |
nonsense |
probably null |
|
R5398:Vmn2r111
|
UTSW |
17 |
22,792,252 (GRCm39) |
start codon destroyed |
probably null |
0.88 |
R5434:Vmn2r111
|
UTSW |
17 |
22,767,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R5462:Vmn2r111
|
UTSW |
17 |
22,767,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R6149:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6149:Vmn2r111
|
UTSW |
17 |
22,767,796 (GRCm39) |
missense |
probably benign |
0.00 |
R6207:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6281:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6282:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6283:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6307:Vmn2r111
|
UTSW |
17 |
22,792,070 (GRCm39) |
missense |
probably benign |
0.00 |
R6323:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6325:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6367:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6368:Vmn2r111
|
UTSW |
17 |
22,790,889 (GRCm39) |
missense |
probably benign |
0.38 |
R6369:Vmn2r111
|
UTSW |
17 |
22,767,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6490:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6546:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6547:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6557:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6654:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6655:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6657:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6659:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6660:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6664:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6798:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6799:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6801:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6893:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6895:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6897:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6922:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6923:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6944:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6945:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7017:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7018:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7024:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7031:Vmn2r111
|
UTSW |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Vmn2r111
|
UTSW |
17 |
22,767,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R7053:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7054:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7055:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7056:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7145:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7146:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7246:Vmn2r111
|
UTSW |
17 |
22,767,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7260:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7327:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7401:Vmn2r111
|
UTSW |
17 |
22,790,067 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7514:Vmn2r111
|
UTSW |
17 |
22,767,380 (GRCm39) |
missense |
probably benign |
0.05 |
R7651:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7781:Vmn2r111
|
UTSW |
17 |
22,789,714 (GRCm39) |
missense |
probably benign |
0.17 |
R7816:Vmn2r111
|
UTSW |
17 |
22,792,083 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7838:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8078:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8080:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8117:Vmn2r111
|
UTSW |
17 |
22,790,469 (GRCm39) |
missense |
probably benign |
0.12 |
R8171:Vmn2r111
|
UTSW |
17 |
22,792,073 (GRCm39) |
missense |
probably benign |
0.10 |
R8195:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8197:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8411:Vmn2r111
|
UTSW |
17 |
22,767,562 (GRCm39) |
missense |
probably benign |
0.03 |
R8539:Vmn2r111
|
UTSW |
17 |
22,790,274 (GRCm39) |
missense |
probably benign |
0.23 |
R8540:Vmn2r111
|
UTSW |
17 |
22,778,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8540:Vmn2r111
|
UTSW |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
R8557:Vmn2r111
|
UTSW |
17 |
22,790,910 (GRCm39) |
nonsense |
probably null |
|
R8720:Vmn2r111
|
UTSW |
17 |
22,792,194 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8729:Vmn2r111
|
UTSW |
17 |
22,767,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9184:Vmn2r111
|
UTSW |
17 |
22,790,822 (GRCm39) |
missense |
probably benign |
|
R9374:Vmn2r111
|
UTSW |
17 |
22,787,859 (GRCm39) |
missense |
probably benign |
0.17 |
R9452:Vmn2r111
|
UTSW |
17 |
22,778,132 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Vmn2r111
|
UTSW |
17 |
22,767,676 (GRCm39) |
missense |
probably damaging |
0.98 |
|