Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
C |
T |
6: 92,885,527 (GRCm39) |
R416Q |
possibly damaging |
Het |
Adgre1 |
C |
A |
17: 57,713,859 (GRCm39) |
D181E |
probably benign |
Het |
Arhgap24 |
T |
C |
5: 103,028,652 (GRCm39) |
S183P |
probably damaging |
Het |
Asb1 |
T |
C |
1: 91,474,748 (GRCm39) |
L90P |
probably damaging |
Het |
Bmp3 |
T |
C |
5: 99,020,209 (GRCm39) |
F211L |
probably benign |
Het |
C8a |
A |
G |
4: 104,703,139 (GRCm39) |
I306T |
probably benign |
Het |
Cdkn3 |
G |
A |
14: 47,007,373 (GRCm39) |
G177R |
probably damaging |
Het |
Chat |
A |
G |
14: 32,170,984 (GRCm39) |
S172P |
probably damaging |
Het |
Chd5 |
CAAGAAGAAGAAGAAGAA |
CAAGAAGAAGAAGAA |
4: 152,438,078 (GRCm39) |
|
probably benign |
Het |
Cyp4a12a |
T |
C |
4: 115,184,420 (GRCm39) |
I265T |
probably damaging |
Het |
Dlst |
T |
A |
12: 85,165,664 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
A |
T |
9: 20,837,716 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
C |
T |
2: 125,205,800 (GRCm39) |
E1066K |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Fstl1 |
T |
A |
16: 37,641,538 (GRCm39) |
S105T |
probably benign |
Het |
Gm19410 |
C |
G |
8: 36,276,518 (GRCm39) |
A1725G |
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,151,215 (GRCm39) |
N119S |
probably damaging |
Het |
Il20 |
T |
A |
1: 130,838,478 (GRCm39) |
D73V |
possibly damaging |
Het |
Insrr |
T |
C |
3: 87,716,608 (GRCm39) |
I612T |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 23,359,105 (GRCm39) |
Y1107C |
probably benign |
Het |
Klhl32 |
A |
G |
4: 24,792,615 (GRCm39) |
|
probably null |
Het |
Krt77 |
C |
A |
15: 101,769,351 (GRCm39) |
R470L |
possibly damaging |
Het |
Muc1 |
T |
C |
3: 89,139,336 (GRCm39) |
Y579H |
probably damaging |
Het |
Myom1 |
T |
G |
17: 71,417,746 (GRCm39) |
D1316E |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,912,538 (GRCm39) |
E1083G |
probably benign |
Het |
Nek9 |
G |
A |
12: 85,359,859 (GRCm39) |
A531V |
probably benign |
Het |
Nlrp12 |
A |
T |
7: 3,290,002 (GRCm39) |
I170N |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,784,002 (GRCm39) |
I1093T |
probably benign |
Het |
Ovch2 |
G |
A |
7: 107,388,318 (GRCm39) |
L421F |
probably damaging |
Het |
Paqr4 |
T |
C |
17: 23,958,968 (GRCm39) |
D11G |
probably damaging |
Het |
Parp8 |
A |
G |
13: 117,014,134 (GRCm39) |
S561P |
probably damaging |
Het |
Pcgf5 |
T |
A |
19: 36,420,306 (GRCm39) |
F179L |
probably damaging |
Het |
Pde4d |
A |
T |
13: 110,084,876 (GRCm39) |
Q422L |
probably damaging |
Het |
Pigs |
T |
A |
11: 78,232,651 (GRCm39) |
V495E |
probably damaging |
Het |
Polh |
C |
T |
17: 46,498,959 (GRCm39) |
R252H |
probably benign |
Het |
Psg28 |
T |
C |
7: 18,160,107 (GRCm39) |
D363G |
possibly damaging |
Het |
Ptgir |
A |
T |
7: 16,640,815 (GRCm39) |
I36F |
possibly damaging |
Het |
Ptprr |
G |
A |
10: 116,072,668 (GRCm39) |
|
probably null |
Het |
Rax |
C |
T |
18: 66,068,418 (GRCm39) |
G229D |
unknown |
Het |
Secisbp2l |
T |
A |
2: 125,615,136 (GRCm39) |
H163L |
probably benign |
Het |
Sf3a2 |
A |
G |
10: 80,637,297 (GRCm39) |
Y45C |
probably damaging |
Het |
Sgo2a |
C |
T |
1: 58,055,775 (GRCm39) |
T653I |
possibly damaging |
Het |
Slc38a9 |
A |
T |
13: 112,806,231 (GRCm39) |
I26F |
probably damaging |
Het |
Slc5a8 |
A |
G |
10: 88,722,436 (GRCm39) |
I90V |
probably benign |
Het |
Slx4 |
G |
A |
16: 3,803,911 (GRCm39) |
H968Y |
possibly damaging |
Het |
Stam2 |
T |
C |
2: 52,599,611 (GRCm39) |
T233A |
probably benign |
Het |
Tln1 |
G |
C |
4: 43,555,052 (GRCm39) |
F259L |
probably damaging |
Het |
Trav4-2 |
G |
A |
14: 53,655,866 (GRCm39) |
V8M |
possibly damaging |
Het |
Ttll5 |
T |
A |
12: 85,878,729 (GRCm39) |
H45Q |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,714,762 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
A |
1: 188,051,217 (GRCm39) |
F234L |
possibly damaging |
Het |
Vmn2r74 |
T |
A |
7: 85,607,526 (GRCm39) |
|
probably null |
Het |
Wdr6 |
CTG |
C |
9: 108,450,994 (GRCm39) |
|
probably null |
Het |
Zfp644 |
A |
G |
5: 106,783,291 (GRCm39) |
S997P |
possibly damaging |
Het |
Zfp853 |
G |
A |
5: 143,274,529 (GRCm39) |
Q364* |
probably null |
Het |
|
Other mutations in Myof |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Myof
|
APN |
19 |
37,949,382 (GRCm39) |
missense |
probably benign |
0.16 |
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 |
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 |
|