Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank3 |
G |
T |
10: 69,740,042 (GRCm39) |
K814N |
probably damaging |
Het |
Anks1b |
A |
G |
10: 89,905,352 (GRCm39) |
H231R |
probably damaging |
Het |
Anks6 |
A |
G |
4: 47,049,164 (GRCm39) |
V247A |
probably benign |
Het |
Antxrl |
A |
G |
14: 33,797,728 (GRCm39) |
N568D |
possibly damaging |
Het |
Ccnl1 |
T |
C |
3: 65,855,373 (GRCm39) |
T366A |
probably benign |
Het |
Ccr2 |
T |
G |
9: 123,906,161 (GRCm39) |
L147R |
probably damaging |
Het |
Cdc40 |
A |
G |
10: 40,720,992 (GRCm39) |
V318A |
probably damaging |
Het |
Cfap61 |
T |
A |
2: 145,792,970 (GRCm39) |
|
probably null |
Het |
Cfap97d2 |
CA |
CAA |
8: 13,784,865 (GRCm39) |
|
probably null |
Het |
Clk3 |
A |
T |
9: 57,669,132 (GRCm39) |
Y31N |
probably damaging |
Het |
Cmya5 |
T |
C |
13: 93,231,644 (GRCm39) |
Y1148C |
probably benign |
Het |
Cntnap5b |
T |
C |
1: 100,311,175 (GRCm39) |
V927A |
probably benign |
Het |
Dync1i1 |
A |
C |
6: 5,913,333 (GRCm39) |
T217P |
probably damaging |
Het |
Elovl4 |
A |
G |
9: 83,667,153 (GRCm39) |
V68A |
probably damaging |
Het |
Ep400 |
C |
A |
5: 110,813,728 (GRCm39) |
K2890N |
probably damaging |
Het |
Fam114a2 |
T |
C |
11: 57,374,897 (GRCm39) |
I481V |
probably benign |
Het |
Fam83e |
A |
G |
7: 45,371,818 (GRCm39) |
T72A |
probably benign |
Het |
Fnip2 |
A |
T |
3: 79,425,418 (GRCm39) |
M59K |
probably benign |
Het |
Lrpprc |
T |
C |
17: 85,030,131 (GRCm39) |
K1089R |
probably benign |
Het |
Mndal |
T |
A |
1: 173,703,249 (GRCm39) |
E52V |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,631,031 (GRCm39) |
F2199I |
possibly damaging |
Het |
Nr1h2 |
A |
T |
7: 44,199,437 (GRCm39) |
L438Q |
probably damaging |
Het |
Or52n2c |
A |
G |
7: 104,574,330 (GRCm39) |
C214R |
probably benign |
Het |
Pet117 |
T |
A |
2: 144,211,019 (GRCm39) |
V13E |
possibly damaging |
Het |
Pnpla8 |
A |
G |
12: 44,330,210 (GRCm39) |
E254G |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,627,003 (GRCm39) |
E1485G |
probably damaging |
Het |
Polr2a |
C |
T |
11: 69,630,293 (GRCm39) |
R1258Q |
probably benign |
Het |
Ptpn4 |
T |
C |
1: 119,700,878 (GRCm39) |
|
probably benign |
Het |
Rapgef2 |
A |
T |
3: 78,993,266 (GRCm39) |
Y889N |
probably damaging |
Het |
Sbf1 |
G |
A |
15: 89,184,572 (GRCm39) |
R1115C |
probably damaging |
Het |
Sfpq |
GCCGCCGCAGCAGCCTCCGCCGCAGCAGCC |
GCCGCCGCAGCAGCC |
4: 126,915,419 (GRCm39) |
|
probably benign |
Het |
Shank2 |
A |
T |
7: 143,645,515 (GRCm39) |
T366S |
probably benign |
Het |
Slc22a23 |
T |
C |
13: 34,489,163 (GRCm39) |
I241V |
probably benign |
Het |
Sox11 |
G |
T |
12: 27,391,493 (GRCm39) |
S305R |
probably damaging |
Het |
Sox21 |
T |
C |
14: 118,472,725 (GRCm39) |
H108R |
possibly damaging |
Het |
Taok1 |
A |
T |
11: 77,446,479 (GRCm39) |
S417T |
probably benign |
Het |
Tg |
C |
T |
15: 66,636,158 (GRCm39) |
R582C |
possibly damaging |
Het |
Traf3 |
T |
C |
12: 111,221,658 (GRCm39) |
V273A |
possibly damaging |
Het |
Tspyl3 |
T |
C |
2: 153,067,203 (GRCm39) |
T12A |
probably benign |
Het |
Vmn2r86 |
A |
T |
10: 130,282,126 (GRCm39) |
I830N |
probably damaging |
Het |
Vps26b |
A |
T |
9: 26,926,613 (GRCm39) |
F129I |
possibly damaging |
Het |
Washc3 |
A |
G |
10: 88,037,714 (GRCm39) |
N24S |
probably damaging |
Het |
Xirp2 |
C |
A |
2: 67,345,201 (GRCm39) |
Q2481K |
probably benign |
Het |
Zfhx4 |
T |
C |
3: 5,478,047 (GRCm39) |
V3554A |
probably damaging |
Het |
|
Other mutations in Myom1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Myom1
|
APN |
17 |
71,433,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00845:Myom1
|
APN |
17 |
71,391,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00904:Myom1
|
APN |
17 |
71,406,944 (GRCm39) |
splice site |
probably benign |
|
IGL00928:Myom1
|
APN |
17 |
71,396,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01025:Myom1
|
APN |
17 |
71,384,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Myom1
|
APN |
17 |
71,408,215 (GRCm39) |
splice site |
probably benign |
|
IGL01588:Myom1
|
APN |
17 |
71,424,432 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01614:Myom1
|
APN |
17 |
71,433,173 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01618:Myom1
|
APN |
17 |
71,406,988 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01619:Myom1
|
APN |
17 |
71,351,471 (GRCm39) |
splice site |
probably benign |
|
IGL01766:Myom1
|
APN |
17 |
71,384,283 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02105:Myom1
|
APN |
17 |
71,354,711 (GRCm39) |
splice site |
probably benign |
|
IGL02122:Myom1
|
APN |
17 |
71,399,132 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02184:Myom1
|
APN |
17 |
71,379,132 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02260:Myom1
|
APN |
17 |
71,415,310 (GRCm39) |
nonsense |
probably null |
|
IGL02486:Myom1
|
APN |
17 |
71,406,939 (GRCm39) |
splice site |
probably benign |
|
IGL02501:Myom1
|
APN |
17 |
71,379,076 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02642:Myom1
|
APN |
17 |
71,408,093 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02677:Myom1
|
APN |
17 |
71,391,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02719:Myom1
|
APN |
17 |
71,413,349 (GRCm39) |
splice site |
probably benign |
|
IGL02945:Myom1
|
APN |
17 |
71,399,088 (GRCm39) |
splice site |
probably benign |
|
IGL03086:Myom1
|
APN |
17 |
71,415,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03218:Myom1
|
APN |
17 |
71,391,311 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0107:Myom1
|
UTSW |
17 |
71,384,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R0130:Myom1
|
UTSW |
17 |
71,352,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R0133:Myom1
|
UTSW |
17 |
71,354,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Myom1
|
UTSW |
17 |
71,344,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Myom1
|
UTSW |
17 |
71,344,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0352:Myom1
|
UTSW |
17 |
71,352,744 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0396:Myom1
|
UTSW |
17 |
71,341,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R0496:Myom1
|
UTSW |
17 |
71,391,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Myom1
|
UTSW |
17 |
71,399,215 (GRCm39) |
splice site |
probably benign |
|
R0511:Myom1
|
UTSW |
17 |
71,391,312 (GRCm39) |
missense |
probably benign |
0.22 |
R0600:Myom1
|
UTSW |
17 |
71,427,643 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0699:Myom1
|
UTSW |
17 |
71,374,308 (GRCm39) |
missense |
probably damaging |
0.98 |
R0791:Myom1
|
UTSW |
17 |
71,428,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Myom1
|
UTSW |
17 |
71,428,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R0963:Myom1
|
UTSW |
17 |
71,384,762 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1324:Myom1
|
UTSW |
17 |
71,359,714 (GRCm39) |
missense |
probably damaging |
0.98 |
R2102:Myom1
|
UTSW |
17 |
71,408,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R2158:Myom1
|
UTSW |
17 |
71,371,592 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2336:Myom1
|
UTSW |
17 |
71,330,189 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2351:Myom1
|
UTSW |
17 |
71,341,574 (GRCm39) |
missense |
probably damaging |
0.98 |
R2442:Myom1
|
UTSW |
17 |
71,417,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Myom1
|
UTSW |
17 |
71,384,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R2892:Myom1
|
UTSW |
17 |
71,341,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Myom1
|
UTSW |
17 |
71,408,215 (GRCm39) |
splice site |
probably benign |
|
R3440:Myom1
|
UTSW |
17 |
71,352,658 (GRCm39) |
splice site |
probably null |
|
R3842:Myom1
|
UTSW |
17 |
71,352,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Myom1
|
UTSW |
17 |
71,399,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R4329:Myom1
|
UTSW |
17 |
71,343,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4594:Myom1
|
UTSW |
17 |
71,407,069 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4873:Myom1
|
UTSW |
17 |
71,379,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Myom1
|
UTSW |
17 |
71,379,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Myom1
|
UTSW |
17 |
71,384,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Myom1
|
UTSW |
17 |
71,406,967 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5540:Myom1
|
UTSW |
17 |
71,416,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R5882:Myom1
|
UTSW |
17 |
71,417,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R5978:Myom1
|
UTSW |
17 |
71,424,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Myom1
|
UTSW |
17 |
71,417,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Myom1
|
UTSW |
17 |
71,417,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Myom1
|
UTSW |
17 |
71,415,690 (GRCm39) |
critical splice donor site |
probably null |
|
R6261:Myom1
|
UTSW |
17 |
71,433,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6284:Myom1
|
UTSW |
17 |
71,329,887 (GRCm39) |
nonsense |
probably null |
|
R6313:Myom1
|
UTSW |
17 |
71,389,483 (GRCm39) |
missense |
probably benign |
|
R6369:Myom1
|
UTSW |
17 |
71,408,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6545:Myom1
|
UTSW |
17 |
71,389,300 (GRCm39) |
missense |
probably benign |
0.00 |
R6738:Myom1
|
UTSW |
17 |
71,407,393 (GRCm39) |
splice site |
probably null |
|
R7168:Myom1
|
UTSW |
17 |
71,396,942 (GRCm39) |
missense |
probably benign |
0.00 |
R7286:Myom1
|
UTSW |
17 |
71,352,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7315:Myom1
|
UTSW |
17 |
71,387,892 (GRCm39) |
critical splice donor site |
probably null |
|
R7672:Myom1
|
UTSW |
17 |
71,391,235 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7789:Myom1
|
UTSW |
17 |
71,424,431 (GRCm39) |
missense |
probably benign |
0.03 |
R7898:Myom1
|
UTSW |
17 |
71,352,747 (GRCm39) |
missense |
probably benign |
0.25 |
R8008:Myom1
|
UTSW |
17 |
71,407,057 (GRCm39) |
missense |
probably benign |
0.30 |
R8152:Myom1
|
UTSW |
17 |
71,391,290 (GRCm39) |
missense |
probably damaging |
0.96 |
R8554:Myom1
|
UTSW |
17 |
71,343,448 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8874:Myom1
|
UTSW |
17 |
71,413,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8981:Myom1
|
UTSW |
17 |
71,391,316 (GRCm39) |
missense |
probably benign |
0.09 |
R9012:Myom1
|
UTSW |
17 |
71,407,103 (GRCm39) |
missense |
probably benign |
0.06 |
R9090:Myom1
|
UTSW |
17 |
71,374,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Myom1
|
UTSW |
17 |
71,343,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R9237:Myom1
|
UTSW |
17 |
71,408,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Myom1
|
UTSW |
17 |
71,374,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R9355:Myom1
|
UTSW |
17 |
71,384,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Myom1
|
UTSW |
17 |
71,343,288 (GRCm39) |
missense |
probably benign |
0.00 |
R9440:Myom1
|
UTSW |
17 |
71,433,329 (GRCm39) |
missense |
probably benign |
0.00 |
R9469:Myom1
|
UTSW |
17 |
71,368,122 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9568:Myom1
|
UTSW |
17 |
71,394,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Myom1
|
UTSW |
17 |
71,412,475 (GRCm39) |
nonsense |
probably null |
|
R9645:Myom1
|
UTSW |
17 |
71,399,204 (GRCm39) |
missense |
probably benign |
0.01 |
X0019:Myom1
|
UTSW |
17 |
71,407,066 (GRCm39) |
missense |
possibly damaging |
0.55 |
|