Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
G |
A |
7: 119,777,085 (GRCm38) |
S345N |
possibly damaging |
Het |
Agk |
A |
T |
6: 40,329,517 (GRCm38) |
T7S |
possibly damaging |
Het |
Ankrd26 |
T |
C |
6: 118,511,663 (GRCm38) |
E1345G |
possibly damaging |
Het |
Atp1a3 |
T |
A |
7: 24,990,515 (GRCm38) |
Y493F |
probably benign |
Het |
Atxn2l |
G |
T |
7: 126,494,211 (GRCm38) |
Y791* |
probably null |
Het |
Cacng8 |
C |
A |
7: 3,415,421 (GRCm38) |
T363K |
probably benign |
Het |
Camkmt |
A |
G |
17: 85,431,493 (GRCm38) |
T216A |
probably benign |
Het |
Cd2ap |
G |
A |
17: 42,830,013 (GRCm38) |
R212* |
probably null |
Het |
Cnppd1 |
A |
G |
1: 75,136,424 (GRCm38) |
L400P |
probably damaging |
Het |
Csmd2 |
C |
A |
4: 128,528,262 (GRCm38) |
D2797E |
|
Het |
Ddx24 |
A |
G |
12: 103,419,450 (GRCm38) |
M298T |
possibly damaging |
Het |
Dpyd |
T |
C |
3: 118,899,284 (GRCm38) |
V359A |
possibly damaging |
Het |
Dscam |
T |
C |
16: 97,056,532 (GRCm38) |
T93A |
probably benign |
Het |
Eif2b3 |
T |
A |
4: 117,052,822 (GRCm38) |
S185T |
probably benign |
Het |
Entpd2 |
T |
A |
2: 25,400,909 (GRCm38) |
I475N |
possibly damaging |
Het |
Ercc2 |
C |
A |
7: 19,394,135 (GRCm38) |
Q715K |
probably benign |
Het |
Fam122a |
T |
A |
19: 24,477,346 (GRCm38) |
E4V |
probably damaging |
Het |
Fam122a |
T |
A |
19: 24,477,124 (GRCm38) |
H78L |
probably benign |
Het |
Fam186b |
T |
C |
15: 99,278,748 (GRCm38) |
R754G |
probably benign |
Het |
Fcgbp |
T |
A |
7: 28,093,436 (GRCm38) |
V955E |
possibly damaging |
Het |
Frrs1 |
T |
C |
3: 116,895,563 (GRCm38) |
V361A |
possibly damaging |
Het |
Gabrr2 |
T |
A |
4: 33,095,284 (GRCm38) |
M391K |
probably benign |
Het |
Gm12394 |
T |
C |
4: 42,792,923 (GRCm38) |
N403S |
possibly damaging |
Het |
Gm3409 |
T |
A |
5: 146,539,547 (GRCm38) |
D169E |
probably benign |
Het |
Gm4779 |
TCGGGGCCGGGGCCGGGGCCG |
TCGGGGCCGGGGCCGGGGCCGGGGCCG |
X: 101,794,171 (GRCm38) |
|
probably benign |
Het |
Greb1l |
C |
G |
18: 10,544,970 (GRCm38) |
Q1433E |
probably damaging |
Het |
Hal |
T |
C |
10: 93,492,561 (GRCm38) |
V233A |
probably benign |
Het |
Ighv1-58 |
A |
T |
12: 115,312,295 (GRCm38) |
N74K |
probably benign |
Het |
Il12rb1 |
A |
G |
8: 70,813,699 (GRCm38) |
I229M |
possibly damaging |
Het |
Il17rd |
T |
C |
14: 27,076,391 (GRCm38) |
I56T |
possibly damaging |
Het |
Itpr1 |
T |
C |
6: 108,542,024 (GRCm38) |
V2708A |
possibly damaging |
Het |
Klhl38 |
G |
A |
15: 58,322,980 (GRCm38) |
R118W |
probably damaging |
Het |
Lmf2 |
C |
A |
15: 89,355,530 (GRCm38) |
|
probably benign |
Het |
Lrrc3b |
T |
C |
14: 15,357,934 (GRCm38) |
Y224C |
probably damaging |
Het |
Med1 |
A |
C |
11: 98,152,808 (GRCm38) |
F599C |
probably benign |
Het |
Mrgprb4 |
A |
G |
7: 48,198,758 (GRCm38) |
S141P |
probably damaging |
Het |
Mst1r |
G |
T |
9: 107,914,790 (GRCm38) |
A842S |
possibly damaging |
Het |
Nos1 |
A |
T |
5: 117,867,905 (GRCm38) |
D230V |
possibly damaging |
Het |
Nppb |
T |
C |
4: 147,986,323 (GRCm38) |
S52P |
probably benign |
Het |
Nqo1 |
A |
G |
8: 107,392,648 (GRCm38) |
I99T |
probably damaging |
Het |
Olfr346 |
T |
A |
2: 36,688,011 (GRCm38) |
M3K |
probably benign |
Het |
Olfr769 |
T |
C |
10: 129,111,699 (GRCm38) |
H242R |
probably damaging |
Het |
Pcdha3 |
G |
A |
18: 36,946,924 (GRCm38) |
E240K |
possibly damaging |
Het |
Plpp7 |
T |
G |
2: 32,096,055 (GRCm38) |
F82V |
probably benign |
Het |
Podxl |
G |
T |
6: 31,524,436 (GRCm38) |
P395T |
probably damaging |
Het |
Prr5l |
T |
A |
2: 101,717,286 (GRCm38) |
D298V |
probably damaging |
Het |
Rad9b |
A |
G |
5: 122,352,614 (GRCm38) |
V13A |
possibly damaging |
Het |
Rasl2-9 |
A |
G |
7: 5,125,740 (GRCm38) |
W64R |
probably damaging |
Het |
Rilp |
G |
T |
11: 75,510,116 (GRCm38) |
|
probably benign |
Het |
Ripor2 |
T |
C |
13: 24,725,001 (GRCm38) |
I1034T |
possibly damaging |
Het |
Rtn4ip1 |
T |
C |
10: 43,936,020 (GRCm38) |
Y338H |
probably damaging |
Het |
Shisa5 |
G |
T |
9: 109,054,884 (GRCm38) |
|
probably benign |
Het |
Slc27a4 |
C |
T |
2: 29,812,932 (GRCm38) |
T591I |
probably null |
Het |
Snx24 |
G |
T |
18: 53,340,172 (GRCm38) |
V63F |
probably damaging |
Het |
Sptbn1 |
A |
T |
11: 30,117,798 (GRCm38) |
Y1805* |
probably null |
Het |
Svep1 |
G |
A |
4: 58,046,587 (GRCm38) |
Q3515* |
probably null |
Het |
Synpo2 |
A |
C |
3: 123,114,053 (GRCm38) |
M538R |
probably benign |
Het |
Tfap2a |
T |
C |
13: 40,721,308 (GRCm38) |
K276E |
probably damaging |
Het |
Tmem158 |
C |
A |
9: 123,260,301 (GRCm38) |
S82I |
probably damaging |
Het |
Tmtc3 |
G |
T |
10: 100,447,474 (GRCm38) |
H740N |
not run |
Het |
Top3a |
A |
T |
11: 60,748,148 (GRCm38) |
F559I |
probably damaging |
Het |
Tysnd1 |
C |
A |
10: 61,696,549 (GRCm38) |
P327T |
possibly damaging |
Het |
Ulk4 |
T |
A |
9: 121,145,059 (GRCm38) |
D969V |
probably benign |
Het |
Vcan |
T |
A |
13: 89,705,266 (GRCm38) |
Y525F |
probably benign |
Het |
Vmn1r127 |
A |
G |
7: 21,319,053 (GRCm38) |
F270S |
probably benign |
Het |
Vmn1r204 |
G |
A |
13: 22,556,805 (GRCm38) |
S202N |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,345,616 (GRCm38) |
I64M |
probably benign |
Het |
Zfp280b |
C |
G |
10: 76,038,703 (GRCm38) |
Q139E |
probably damaging |
Het |
Zfp322a |
C |
T |
13: 23,357,144 (GRCm38) |
G143S |
probably benign |
Het |
Zfp322a |
C |
A |
13: 23,357,143 (GRCm38) |
G143V |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,282,984 (GRCm38) |
V476D |
probably benign |
Het |
Zkscan6 |
A |
T |
11: 65,828,225 (GRCm38) |
H357L |
probably benign |
Het |
|
Other mutations in Myo3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01014:Myo3a
|
APN |
2 |
22,332,473 (GRCm38) |
missense |
probably benign |
0.42 |
IGL01307:Myo3a
|
APN |
2 |
22,558,289 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01413:Myo3a
|
APN |
2 |
22,297,600 (GRCm38) |
missense |
probably benign |
0.25 |
IGL01655:Myo3a
|
APN |
2 |
22,423,326 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01767:Myo3a
|
APN |
2 |
22,423,222 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01803:Myo3a
|
APN |
2 |
22,241,115 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01969:Myo3a
|
APN |
2 |
22,297,688 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02043:Myo3a
|
APN |
2 |
22,399,965 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02124:Myo3a
|
APN |
2 |
22,577,526 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02174:Myo3a
|
APN |
2 |
22,332,393 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02649:Myo3a
|
APN |
2 |
22,323,607 (GRCm38) |
missense |
probably benign |
|
IGL02976:Myo3a
|
APN |
2 |
22,542,452 (GRCm38) |
nonsense |
probably null |
|
IGL03328:Myo3a
|
APN |
2 |
22,578,198 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03376:Myo3a
|
APN |
2 |
22,600,074 (GRCm38) |
splice site |
probably benign |
|
lose
|
UTSW |
2 |
22,558,320 (GRCm38) |
nonsense |
probably null |
|
snooze
|
UTSW |
2 |
22,282,634 (GRCm38) |
missense |
probably damaging |
0.99 |
A5278:Myo3a
|
UTSW |
2 |
22,323,653 (GRCm38) |
missense |
probably benign |
0.27 |
PIT4445001:Myo3a
|
UTSW |
2 |
22,542,415 (GRCm38) |
missense |
possibly damaging |
0.64 |
R0008:Myo3a
|
UTSW |
2 |
22,579,741 (GRCm38) |
missense |
probably damaging |
0.99 |
R0099:Myo3a
|
UTSW |
2 |
22,245,598 (GRCm38) |
missense |
probably benign |
0.03 |
R0103:Myo3a
|
UTSW |
2 |
22,544,322 (GRCm38) |
splice site |
probably benign |
|
R0103:Myo3a
|
UTSW |
2 |
22,544,322 (GRCm38) |
splice site |
probably benign |
|
R0212:Myo3a
|
UTSW |
2 |
22,291,848 (GRCm38) |
missense |
probably damaging |
1.00 |
R0281:Myo3a
|
UTSW |
2 |
22,245,598 (GRCm38) |
missense |
probably benign |
0.03 |
R0282:Myo3a
|
UTSW |
2 |
22,245,598 (GRCm38) |
missense |
probably benign |
0.03 |
R0492:Myo3a
|
UTSW |
2 |
22,323,636 (GRCm38) |
missense |
possibly damaging |
0.46 |
R0498:Myo3a
|
UTSW |
2 |
22,577,429 (GRCm38) |
missense |
possibly damaging |
0.74 |
R0594:Myo3a
|
UTSW |
2 |
22,544,332 (GRCm38) |
splice site |
probably benign |
|
R0609:Myo3a
|
UTSW |
2 |
22,396,299 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0609:Myo3a
|
UTSW |
2 |
22,333,513 (GRCm38) |
missense |
probably benign |
0.29 |
R0827:Myo3a
|
UTSW |
2 |
22,558,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R0968:Myo3a
|
UTSW |
2 |
22,558,289 (GRCm38) |
missense |
probably damaging |
1.00 |
R1157:Myo3a
|
UTSW |
2 |
22,542,414 (GRCm38) |
critical splice acceptor site |
probably null |
|
R1301:Myo3a
|
UTSW |
2 |
22,267,095 (GRCm38) |
splice site |
probably benign |
|
R1352:Myo3a
|
UTSW |
2 |
22,323,675 (GRCm38) |
critical splice donor site |
probably null |
|
R1443:Myo3a
|
UTSW |
2 |
22,282,626 (GRCm38) |
missense |
probably damaging |
0.99 |
R1465:Myo3a
|
UTSW |
2 |
22,577,927 (GRCm38) |
missense |
probably benign |
0.00 |
R1465:Myo3a
|
UTSW |
2 |
22,577,927 (GRCm38) |
missense |
probably benign |
0.00 |
R1517:Myo3a
|
UTSW |
2 |
22,282,634 (GRCm38) |
missense |
probably damaging |
0.99 |
R1565:Myo3a
|
UTSW |
2 |
22,340,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R1712:Myo3a
|
UTSW |
2 |
22,564,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R1722:Myo3a
|
UTSW |
2 |
22,399,827 (GRCm38) |
missense |
probably benign |
0.03 |
R1822:Myo3a
|
UTSW |
2 |
22,340,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R1823:Myo3a
|
UTSW |
2 |
22,340,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R1824:Myo3a
|
UTSW |
2 |
22,396,243 (GRCm38) |
missense |
probably benign |
|
R1837:Myo3a
|
UTSW |
2 |
22,577,592 (GRCm38) |
missense |
possibly damaging |
0.76 |
R1867:Myo3a
|
UTSW |
2 |
22,399,846 (GRCm38) |
missense |
probably benign |
0.00 |
R1917:Myo3a
|
UTSW |
2 |
22,291,922 (GRCm38) |
missense |
probably damaging |
1.00 |
R1920:Myo3a
|
UTSW |
2 |
22,564,996 (GRCm38) |
missense |
probably benign |
0.02 |
R1937:Myo3a
|
UTSW |
2 |
22,396,315 (GRCm38) |
missense |
probably damaging |
1.00 |
R1954:Myo3a
|
UTSW |
2 |
22,241,226 (GRCm38) |
missense |
probably damaging |
1.00 |
R1988:Myo3a
|
UTSW |
2 |
22,578,128 (GRCm38) |
missense |
possibly damaging |
0.86 |
R2091:Myo3a
|
UTSW |
2 |
22,333,677 (GRCm38) |
missense |
probably damaging |
0.99 |
R2115:Myo3a
|
UTSW |
2 |
22,245,531 (GRCm38) |
missense |
probably damaging |
1.00 |
R2125:Myo3a
|
UTSW |
2 |
22,578,174 (GRCm38) |
missense |
probably benign |
0.42 |
R2126:Myo3a
|
UTSW |
2 |
22,578,174 (GRCm38) |
missense |
probably benign |
0.42 |
R2216:Myo3a
|
UTSW |
2 |
22,577,771 (GRCm38) |
missense |
probably benign |
0.00 |
R2413:Myo3a
|
UTSW |
2 |
22,577,912 (GRCm38) |
missense |
probably benign |
0.00 |
R2964:Myo3a
|
UTSW |
2 |
22,340,256 (GRCm38) |
missense |
possibly damaging |
0.90 |
R3196:Myo3a
|
UTSW |
2 |
22,399,868 (GRCm38) |
missense |
possibly damaging |
0.86 |
R3837:Myo3a
|
UTSW |
2 |
22,565,109 (GRCm38) |
splice site |
probably benign |
|
R3905:Myo3a
|
UTSW |
2 |
22,558,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R3926:Myo3a
|
UTSW |
2 |
22,565,041 (GRCm38) |
missense |
probably damaging |
0.99 |
R4014:Myo3a
|
UTSW |
2 |
22,578,170 (GRCm38) |
missense |
possibly damaging |
0.76 |
R4015:Myo3a
|
UTSW |
2 |
22,578,170 (GRCm38) |
missense |
possibly damaging |
0.76 |
R4017:Myo3a
|
UTSW |
2 |
22,578,170 (GRCm38) |
missense |
possibly damaging |
0.76 |
R4043:Myo3a
|
UTSW |
2 |
22,333,539 (GRCm38) |
splice site |
probably benign |
|
R4044:Myo3a
|
UTSW |
2 |
22,577,700 (GRCm38) |
missense |
probably damaging |
0.99 |
R4057:Myo3a
|
UTSW |
2 |
22,266,160 (GRCm38) |
missense |
probably benign |
0.01 |
R4192:Myo3a
|
UTSW |
2 |
22,407,377 (GRCm38) |
missense |
probably damaging |
1.00 |
R4282:Myo3a
|
UTSW |
2 |
22,340,278 (GRCm38) |
missense |
probably benign |
0.14 |
R4321:Myo3a
|
UTSW |
2 |
22,267,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R4393:Myo3a
|
UTSW |
2 |
22,577,854 (GRCm38) |
missense |
probably damaging |
0.99 |
R4398:Myo3a
|
UTSW |
2 |
22,577,842 (GRCm38) |
missense |
probably benign |
|
R4446:Myo3a
|
UTSW |
2 |
22,600,137 (GRCm38) |
missense |
probably damaging |
1.00 |
R4685:Myo3a
|
UTSW |
2 |
22,407,422 (GRCm38) |
missense |
probably damaging |
1.00 |
R5032:Myo3a
|
UTSW |
2 |
22,282,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R5096:Myo3a
|
UTSW |
2 |
22,574,242 (GRCm38) |
missense |
probably benign |
0.16 |
R5183:Myo3a
|
UTSW |
2 |
22,578,158 (GRCm38) |
missense |
probably benign |
0.05 |
R5458:Myo3a
|
UTSW |
2 |
22,245,550 (GRCm38) |
missense |
probably damaging |
1.00 |
R5502:Myo3a
|
UTSW |
2 |
22,558,369 (GRCm38) |
missense |
probably damaging |
1.00 |
R5522:Myo3a
|
UTSW |
2 |
22,574,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R6462:Myo3a
|
UTSW |
2 |
22,558,411 (GRCm38) |
missense |
probably damaging |
1.00 |
R6479:Myo3a
|
UTSW |
2 |
22,577,865 (GRCm38) |
missense |
probably benign |
0.00 |
R6513:Myo3a
|
UTSW |
2 |
22,407,332 (GRCm38) |
missense |
probably damaging |
1.00 |
R6520:Myo3a
|
UTSW |
2 |
22,399,926 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6602:Myo3a
|
UTSW |
2 |
22,577,787 (GRCm38) |
missense |
probably damaging |
0.96 |
R6671:Myo3a
|
UTSW |
2 |
22,294,522 (GRCm38) |
missense |
probably damaging |
1.00 |
R6743:Myo3a
|
UTSW |
2 |
22,361,664 (GRCm38) |
missense |
probably benign |
0.24 |
R6865:Myo3a
|
UTSW |
2 |
22,574,301 (GRCm38) |
missense |
probably benign |
0.00 |
R6961:Myo3a
|
UTSW |
2 |
22,245,558 (GRCm38) |
missense |
probably benign |
0.00 |
R7001:Myo3a
|
UTSW |
2 |
22,332,377 (GRCm38) |
missense |
probably benign |
0.04 |
R7215:Myo3a
|
UTSW |
2 |
22,245,567 (GRCm38) |
missense |
possibly damaging |
0.78 |
R7318:Myo3a
|
UTSW |
2 |
22,558,320 (GRCm38) |
nonsense |
probably null |
|
R7447:Myo3a
|
UTSW |
2 |
22,544,426 (GRCm38) |
missense |
probably benign |
0.27 |
R7456:Myo3a
|
UTSW |
2 |
22,407,444 (GRCm38) |
missense |
probably benign |
0.08 |
R7528:Myo3a
|
UTSW |
2 |
22,266,114 (GRCm38) |
nonsense |
probably null |
|
R7731:Myo3a
|
UTSW |
2 |
22,282,589 (GRCm38) |
missense |
probably damaging |
1.00 |
R7768:Myo3a
|
UTSW |
2 |
22,241,143 (GRCm38) |
missense |
probably damaging |
0.99 |
R8054:Myo3a
|
UTSW |
2 |
22,574,317 (GRCm38) |
missense |
probably benign |
0.00 |
R8140:Myo3a
|
UTSW |
2 |
22,407,346 (GRCm38) |
missense |
probably damaging |
1.00 |
R8143:Myo3a
|
UTSW |
2 |
22,282,665 (GRCm38) |
critical splice donor site |
probably null |
|
R8346:Myo3a
|
UTSW |
2 |
22,558,422 (GRCm38) |
critical splice donor site |
probably null |
|
R8421:Myo3a
|
UTSW |
2 |
22,362,124 (GRCm38) |
missense |
probably benign |
0.07 |
R8495:Myo3a
|
UTSW |
2 |
22,396,273 (GRCm38) |
missense |
probably damaging |
0.96 |
R8551:Myo3a
|
UTSW |
2 |
22,332,466 (GRCm38) |
missense |
probably benign |
0.00 |
R8708:Myo3a
|
UTSW |
2 |
22,291,796 (GRCm38) |
splice site |
probably benign |
|
R8757:Myo3a
|
UTSW |
2 |
22,558,307 (GRCm38) |
missense |
possibly damaging |
0.49 |
R8759:Myo3a
|
UTSW |
2 |
22,558,307 (GRCm38) |
missense |
possibly damaging |
0.49 |
R8779:Myo3a
|
UTSW |
2 |
22,245,593 (GRCm38) |
nonsense |
probably null |
|
R8828:Myo3a
|
UTSW |
2 |
22,241,053 (GRCm38) |
missense |
probably benign |
0.01 |
R8910:Myo3a
|
UTSW |
2 |
22,574,268 (GRCm38) |
missense |
probably benign |
0.01 |
R8916:Myo3a
|
UTSW |
2 |
22,567,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R8926:Myo3a
|
UTSW |
2 |
22,396,263 (GRCm38) |
missense |
possibly damaging |
0.95 |
R9028:Myo3a
|
UTSW |
2 |
22,600,087 (GRCm38) |
missense |
possibly damaging |
0.79 |
R9046:Myo3a
|
UTSW |
2 |
22,558,355 (GRCm38) |
missense |
probably damaging |
0.99 |
R9120:Myo3a
|
UTSW |
2 |
22,544,426 (GRCm38) |
missense |
probably benign |
0.27 |
R9153:Myo3a
|
UTSW |
2 |
22,399,933 (GRCm38) |
missense |
probably benign |
0.02 |
R9191:Myo3a
|
UTSW |
2 |
22,579,829 (GRCm38) |
missense |
probably benign |
0.24 |
R9258:Myo3a
|
UTSW |
2 |
22,577,533 (GRCm38) |
missense |
possibly damaging |
0.60 |
R9436:Myo3a
|
UTSW |
2 |
22,407,424 (GRCm38) |
nonsense |
probably null |
|
R9464:Myo3a
|
UTSW |
2 |
22,227,572 (GRCm38) |
start gained |
probably benign |
|
R9487:Myo3a
|
UTSW |
2 |
22,241,051 (GRCm38) |
missense |
probably benign |
|
R9719:Myo3a
|
UTSW |
2 |
22,544,455 (GRCm38) |
missense |
probably benign |
0.02 |
R9799:Myo3a
|
UTSW |
2 |
22,600,169 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Myo3a
|
UTSW |
2 |
22,618,140 (GRCm38) |
missense |
possibly damaging |
0.58 |
|