Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd46 |
T |
C |
15: 36,486,113 (GRCm39) |
T47A |
possibly damaging |
Het |
Asxl3 |
T |
G |
18: 22,656,385 (GRCm39) |
V1465G |
probably damaging |
Het |
Celsr3 |
A |
T |
9: 108,711,756 (GRCm39) |
D1657V |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,714,603 (GRCm39) |
H1995R |
probably benign |
Het |
Cimip2b |
G |
A |
4: 43,427,814 (GRCm39) |
T170I |
possibly damaging |
Het |
Cntn6 |
G |
A |
6: 104,705,335 (GRCm39) |
|
probably benign |
Het |
Def6 |
C |
T |
17: 28,426,838 (GRCm39) |
L8F |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,722,441 (GRCm39) |
K1940* |
probably null |
Het |
Dock10 |
A |
G |
1: 80,612,015 (GRCm39) |
|
probably benign |
Het |
Fam72a |
A |
G |
1: 131,461,650 (GRCm39) |
I112V |
probably benign |
Het |
Fgl1 |
A |
T |
8: 41,650,008 (GRCm39) |
W258R |
probably damaging |
Het |
Ints6l |
G |
T |
X: 55,542,104 (GRCm39) |
|
probably benign |
Het |
Lifr |
A |
T |
15: 7,220,643 (GRCm39) |
N1091I |
probably damaging |
Het |
Mga |
T |
C |
2: 119,762,309 (GRCm39) |
I1100T |
possibly damaging |
Het |
Mrpl40 |
T |
A |
16: 18,691,294 (GRCm39) |
M139L |
probably benign |
Het |
Or2m12 |
T |
A |
16: 19,104,909 (GRCm39) |
T195S |
probably damaging |
Het |
Pcdhb5 |
T |
C |
18: 37,455,992 (GRCm39) |
F791L |
probably damaging |
Het |
Prss29 |
T |
C |
17: 25,540,113 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
A |
G |
10: 58,299,900 (GRCm39) |
|
probably null |
Het |
Serpinb9e |
A |
G |
13: 33,439,108 (GRCm39) |
K178R |
probably damaging |
Het |
Shtn1 |
A |
G |
19: 59,016,601 (GRCm39) |
S233P |
probably damaging |
Het |
Smpd1 |
G |
A |
7: 105,204,549 (GRCm39) |
V143M |
possibly damaging |
Het |
Terb1 |
G |
A |
8: 105,199,646 (GRCm39) |
H433Y |
probably benign |
Het |
Traf6 |
C |
T |
2: 101,520,443 (GRCm39) |
Q164* |
probably null |
Het |
Trip12 |
C |
A |
1: 84,792,631 (GRCm39) |
R4L |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,693,879 (GRCm39) |
P208S |
possibly damaging |
Het |
Ube2c |
T |
C |
2: 164,613,232 (GRCm39) |
I50T |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,200,775 (GRCm39) |
D1174G |
probably damaging |
Het |
Vmn2r121 |
T |
G |
X: 123,041,997 (GRCm39) |
M387L |
probably benign |
Het |
Vmn2r18 |
T |
A |
5: 151,510,229 (GRCm39) |
N48I |
probably benign |
Het |
Zc3h15 |
T |
C |
2: 83,490,517 (GRCm39) |
L217P |
probably damaging |
Het |
Zyg11a |
T |
A |
4: 108,062,414 (GRCm39) |
E129V |
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 |
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 |
|
R6933:Myom1
|
UTSW |
17 |
71,359,666 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|