Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss1 |
T |
C |
2: 150,461,606 (GRCm39) |
E659G |
probably benign |
Het |
Adgrg6 |
A |
C |
10: 14,411,703 (GRCm39) |
|
probably benign |
Het |
Als2cl |
A |
G |
9: 110,718,227 (GRCm39) |
K323E |
possibly damaging |
Het |
Atm |
A |
C |
9: 53,424,416 (GRCm39) |
S628R |
probably benign |
Het |
Baz2a |
T |
C |
10: 127,950,395 (GRCm39) |
V443A |
probably benign |
Het |
Bclaf3 |
T |
A |
X: 158,341,357 (GRCm39) |
F545Y |
probably benign |
Het |
Calcr |
T |
C |
6: 3,717,196 (GRCm39) |
Y88C |
probably damaging |
Het |
Ccdc178 |
C |
T |
18: 22,278,501 (GRCm39) |
|
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,875,153 (GRCm39) |
T312A |
probably benign |
Het |
Chrnd |
G |
A |
1: 87,120,649 (GRCm39) |
W91* |
probably null |
Het |
Cntln |
T |
C |
4: 84,897,652 (GRCm39) |
F413S |
probably benign |
Het |
Ctsq |
A |
T |
13: 61,183,998 (GRCm39) |
I308N |
probably damaging |
Het |
Cyp2d34 |
A |
T |
15: 82,501,736 (GRCm39) |
V258D |
probably damaging |
Het |
Dnajc13 |
G |
A |
9: 104,039,979 (GRCm39) |
P2044S |
probably benign |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Hps6 |
A |
T |
19: 45,992,099 (GRCm39) |
D12V |
probably damaging |
Het |
Hpse |
T |
C |
5: 100,846,865 (GRCm39) |
D188G |
probably benign |
Het |
Id2 |
C |
A |
12: 25,145,355 (GRCm39) |
E123* |
probably null |
Het |
Ints10 |
C |
T |
8: 69,271,985 (GRCm39) |
P562L |
probably damaging |
Het |
Kctd10 |
G |
A |
5: 114,505,410 (GRCm39) |
R195C |
probably damaging |
Het |
Kel |
A |
C |
6: 41,665,509 (GRCm39) |
L537R |
probably damaging |
Het |
Kif19a |
T |
C |
11: 114,675,599 (GRCm39) |
V357A |
probably damaging |
Het |
Lrrtm3 |
A |
T |
10: 63,924,988 (GRCm39) |
S60T |
probably damaging |
Het |
Naa35 |
A |
T |
13: 59,778,485 (GRCm39) |
I669F |
probably benign |
Het |
Or8g2b |
A |
T |
9: 39,751,002 (GRCm39) |
I91F |
probably benign |
Het |
Or8g53 |
A |
G |
9: 39,683,407 (GRCm39) |
S230P |
possibly damaging |
Het |
Pclo |
G |
T |
5: 14,728,035 (GRCm39) |
|
probably benign |
Het |
Pik3c3 |
C |
T |
18: 30,407,417 (GRCm39) |
S55F |
probably damaging |
Het |
Prdm6 |
T |
G |
18: 53,673,300 (GRCm39) |
D153E |
possibly damaging |
Het |
Rnf183 |
T |
C |
4: 62,346,610 (GRCm39) |
T63A |
probably benign |
Het |
Samd4b |
A |
C |
7: 28,101,302 (GRCm39) |
I108S |
probably damaging |
Het |
Slc9a7 |
T |
C |
X: 19,972,260 (GRCm39) |
D708G |
possibly damaging |
Het |
Stim2 |
A |
G |
5: 54,210,835 (GRCm39) |
D90G |
probably benign |
Het |
Tmem52b |
A |
G |
6: 129,493,678 (GRCm39) |
D97G |
probably damaging |
Het |
Tnfsf15 |
T |
C |
4: 63,652,518 (GRCm39) |
R98G |
probably benign |
Het |
Uxs1 |
C |
T |
1: 43,796,173 (GRCm39) |
V310I |
probably benign |
Het |
Vcan |
A |
C |
13: 89,873,425 (GRCm39) |
M143R |
probably damaging |
Het |
Vmn2r93 |
T |
C |
17: 18,546,504 (GRCm39) |
F792S |
probably damaging |
Het |
Zfp455 |
T |
C |
13: 67,355,962 (GRCm39) |
I345T |
probably benign |
Het |
Zfp938 |
A |
T |
10: 82,062,317 (GRCm39) |
M101K |
probably benign |
Het |
Zkscan2 |
A |
G |
7: 123,079,195 (GRCm39) |
S921P |
probably damaging |
Het |
|
Other mutations in Myof |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00764:Myof
|
APN |
19 |
37,963,371 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00801:Myof
|
APN |
19 |
37,974,521 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01084:Myof
|
APN |
19 |
37,924,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01368:Myof
|
APN |
19 |
37,924,905 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01472:Myof
|
APN |
19 |
37,911,524 (GRCm39) |
missense |
probably benign |
|
IGL01785:Myof
|
APN |
19 |
37,968,871 (GRCm39) |
nonsense |
probably null |
|
IGL02205:Myof
|
APN |
19 |
37,913,083 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Myof
|
APN |
19 |
37,963,311 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02268:Myof
|
APN |
19 |
37,942,877 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02339:Myof
|
APN |
19 |
37,960,661 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02433:Myof
|
APN |
19 |
37,960,641 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02481:Myof
|
APN |
19 |
37,926,361 (GRCm39) |
nonsense |
probably null |
|
IGL02536:Myof
|
APN |
19 |
37,938,103 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02682:Myof
|
APN |
19 |
37,909,929 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02732:Myof
|
APN |
19 |
37,966,164 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02887:Myof
|
APN |
19 |
37,909,227 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03114:Myof
|
APN |
19 |
37,892,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03137:Myof
|
APN |
19 |
37,963,337 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03340:Myof
|
APN |
19 |
37,899,607 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4791001:Myof
|
UTSW |
19 |
37,971,406 (GRCm39) |
critical splice donor site |
probably null |
|
R0024:Myof
|
UTSW |
19 |
37,904,188 (GRCm39) |
missense |
probably damaging |
0.98 |
R0140:Myof
|
UTSW |
19 |
37,940,004 (GRCm39) |
nonsense |
probably null |
|
R0309:Myof
|
UTSW |
19 |
37,969,714 (GRCm39) |
missense |
probably benign |
0.12 |
R0330:Myof
|
UTSW |
19 |
37,924,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0345:Myof
|
UTSW |
19 |
38,012,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0349:Myof
|
UTSW |
19 |
37,899,417 (GRCm39) |
missense |
probably damaging |
0.99 |
R0463:Myof
|
UTSW |
19 |
37,904,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Myof
|
UTSW |
19 |
37,889,725 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0512:Myof
|
UTSW |
19 |
37,942,972 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0608:Myof
|
UTSW |
19 |
37,904,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Myof
|
UTSW |
19 |
37,969,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R1081:Myof
|
UTSW |
19 |
37,974,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R1196:Myof
|
UTSW |
19 |
37,899,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1243:Myof
|
UTSW |
19 |
37,924,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1371:Myof
|
UTSW |
19 |
37,892,116 (GRCm39) |
splice site |
probably benign |
|
R1381:Myof
|
UTSW |
19 |
37,983,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R1419:Myof
|
UTSW |
19 |
37,890,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1527:Myof
|
UTSW |
19 |
37,913,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Myof
|
UTSW |
19 |
37,931,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1864:Myof
|
UTSW |
19 |
37,975,153 (GRCm39) |
missense |
probably benign |
|
R1914:Myof
|
UTSW |
19 |
37,966,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Myof
|
UTSW |
19 |
37,966,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Myof
|
UTSW |
19 |
37,934,082 (GRCm39) |
missense |
probably damaging |
0.99 |
R2062:Myof
|
UTSW |
19 |
37,904,194 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2144:Myof
|
UTSW |
19 |
37,969,669 (GRCm39) |
critical splice donor site |
probably null |
|
R2243:Myof
|
UTSW |
19 |
37,889,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R2339:Myof
|
UTSW |
19 |
37,926,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Myof
|
UTSW |
19 |
37,892,291 (GRCm39) |
missense |
probably benign |
0.13 |
R2880:Myof
|
UTSW |
19 |
37,911,473 (GRCm39) |
missense |
probably benign |
0.04 |
R3418:Myof
|
UTSW |
19 |
37,911,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R3967:Myof
|
UTSW |
19 |
38,011,058 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3967:Myof
|
UTSW |
19 |
37,889,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R3970:Myof
|
UTSW |
19 |
38,011,058 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3970:Myof
|
UTSW |
19 |
37,889,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4238:Myof
|
UTSW |
19 |
37,911,456 (GRCm39) |
nonsense |
probably null |
|
R4405:Myof
|
UTSW |
19 |
37,911,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R4406:Myof
|
UTSW |
19 |
37,911,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R4407:Myof
|
UTSW |
19 |
37,911,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R4408:Myof
|
UTSW |
19 |
37,911,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R4561:Myof
|
UTSW |
19 |
37,911,438 (GRCm39) |
missense |
probably benign |
|
R4606:Myof
|
UTSW |
19 |
37,955,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Myof
|
UTSW |
19 |
37,938,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Myof
|
UTSW |
19 |
37,934,186 (GRCm39) |
missense |
probably benign |
0.24 |
R4802:Myof
|
UTSW |
19 |
37,934,186 (GRCm39) |
missense |
probably benign |
0.24 |
R4812:Myof
|
UTSW |
19 |
37,905,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Myof
|
UTSW |
19 |
37,930,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Myof
|
UTSW |
19 |
37,924,300 (GRCm39) |
missense |
probably damaging |
0.97 |
R4966:Myof
|
UTSW |
19 |
37,924,300 (GRCm39) |
missense |
probably damaging |
0.97 |
R5069:Myof
|
UTSW |
19 |
37,893,773 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5181:Myof
|
UTSW |
19 |
37,921,071 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5376:Myof
|
UTSW |
19 |
37,904,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Myof
|
UTSW |
19 |
37,941,435 (GRCm39) |
missense |
probably damaging |
0.98 |
R5543:Myof
|
UTSW |
19 |
37,969,778 (GRCm39) |
missense |
probably benign |
0.00 |
R5626:Myof
|
UTSW |
19 |
37,911,438 (GRCm39) |
missense |
probably benign |
|
R5865:Myof
|
UTSW |
19 |
37,899,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R5919:Myof
|
UTSW |
19 |
38,012,818 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5924:Myof
|
UTSW |
19 |
37,971,421 (GRCm39) |
missense |
probably damaging |
0.97 |
R5997:Myof
|
UTSW |
19 |
37,893,747 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5999:Myof
|
UTSW |
19 |
37,928,304 (GRCm39) |
nonsense |
probably null |
|
R6039:Myof
|
UTSW |
19 |
37,966,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Myof
|
UTSW |
19 |
37,966,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Myof
|
UTSW |
19 |
37,913,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Myof
|
UTSW |
19 |
38,012,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6057:Myof
|
UTSW |
19 |
37,915,429 (GRCm39) |
critical splice donor site |
probably null |
|
R6089:Myof
|
UTSW |
19 |
37,955,508 (GRCm39) |
missense |
probably benign |
0.37 |
R6195:Myof
|
UTSW |
19 |
37,901,805 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6478:Myof
|
UTSW |
19 |
37,892,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R6545:Myof
|
UTSW |
19 |
37,930,745 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6655:Myof
|
UTSW |
19 |
37,923,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R6715:Myof
|
UTSW |
19 |
37,956,794 (GRCm39) |
missense |
probably benign |
0.04 |
R6737:Myof
|
UTSW |
19 |
37,931,962 (GRCm39) |
missense |
probably benign |
0.01 |
R6837:Myof
|
UTSW |
19 |
37,911,404 (GRCm39) |
critical splice donor site |
probably null |
|
R7096:Myof
|
UTSW |
19 |
37,924,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R7308:Myof
|
UTSW |
19 |
37,899,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R7328:Myof
|
UTSW |
19 |
37,904,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Myof
|
UTSW |
19 |
37,939,939 (GRCm39) |
nonsense |
probably null |
|
R7554:Myof
|
UTSW |
19 |
37,942,958 (GRCm39) |
missense |
probably benign |
0.09 |
R7759:Myof
|
UTSW |
19 |
37,928,346 (GRCm39) |
missense |
probably benign |
0.00 |
R7779:Myof
|
UTSW |
19 |
37,927,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R8116:Myof
|
UTSW |
19 |
37,921,167 (GRCm39) |
missense |
probably damaging |
0.99 |
R8264:Myof
|
UTSW |
19 |
37,909,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Myof
|
UTSW |
19 |
37,983,872 (GRCm39) |
missense |
probably benign |
|
R8756:Myof
|
UTSW |
19 |
37,928,400 (GRCm39) |
missense |
probably benign |
|
R8777:Myof
|
UTSW |
19 |
37,968,841 (GRCm39) |
missense |
probably benign |
0.01 |
R8777-TAIL:Myof
|
UTSW |
19 |
37,968,841 (GRCm39) |
missense |
probably benign |
0.01 |
R8835:Myof
|
UTSW |
19 |
37,955,547 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9046:Myof
|
UTSW |
19 |
37,923,112 (GRCm39) |
intron |
probably benign |
|
R9396:Myof
|
UTSW |
19 |
37,923,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9415:Myof
|
UTSW |
19 |
37,941,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R9450:Myof
|
UTSW |
19 |
37,949,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Myof
|
UTSW |
19 |
37,966,096 (GRCm39) |
critical splice donor site |
probably null |
|
R9537:Myof
|
UTSW |
19 |
37,896,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Myof
|
UTSW |
19 |
38,031,737 (GRCm39) |
missense |
probably damaging |
0.99 |
R9616:Myof
|
UTSW |
19 |
37,923,263 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9751:Myof
|
UTSW |
19 |
37,924,818 (GRCm39) |
missense |
probably benign |
|
X0024:Myof
|
UTSW |
19 |
37,963,045 (GRCm39) |
missense |
probably benign |
0.14 |
|