Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
G |
A |
4: 144,503,991 (GRCm39) |
R387C |
probably benign |
Het |
Agbl1 |
A |
T |
7: 76,068,470 (GRCm39) |
E93D |
possibly damaging |
Het |
Akap10 |
C |
A |
11: 61,806,327 (GRCm39) |
V134F |
possibly damaging |
Het |
Bnc1 |
T |
C |
7: 81,623,821 (GRCm39) |
I469V |
possibly damaging |
Het |
Bod1l |
T |
A |
5: 41,978,888 (GRCm39) |
I809L |
possibly damaging |
Het |
Dicer1 |
T |
A |
12: 104,696,447 (GRCm39) |
E118V |
probably damaging |
Het |
Dmbt1 |
T |
C |
7: 130,648,292 (GRCm39) |
F274S |
probably benign |
Het |
Dnaaf2 |
T |
G |
12: 69,243,418 (GRCm39) |
T548P |
possibly damaging |
Het |
Dysf |
G |
A |
6: 84,163,491 (GRCm39) |
|
probably null |
Het |
Fchsd2 |
A |
G |
7: 100,883,092 (GRCm39) |
N240S |
probably benign |
Het |
Foxb1 |
T |
C |
9: 69,667,146 (GRCm39) |
Y128C |
probably damaging |
Het |
Fxr2 |
A |
T |
11: 69,532,896 (GRCm39) |
K158M |
possibly damaging |
Het |
Golga4 |
C |
A |
9: 118,385,972 (GRCm39) |
D1031E |
probably benign |
Het |
Hbb-bs |
T |
C |
7: 103,477,018 (GRCm39) |
D22G |
possibly damaging |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hnrnpul2 |
T |
A |
19: 8,798,001 (GRCm39) |
M119K |
probably benign |
Het |
Kif18a |
C |
A |
2: 109,128,452 (GRCm39) |
H369Q |
probably damaging |
Het |
Klhdc10 |
A |
G |
6: 30,449,558 (GRCm39) |
T207A |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,022,161 (GRCm39) |
C540R |
possibly damaging |
Het |
Lilrb4b |
A |
T |
10: 51,357,704 (GRCm39) |
N133Y |
possibly damaging |
Het |
Lrrc31 |
T |
A |
3: 30,739,179 (GRCm39) |
|
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Nlrp2 |
C |
T |
7: 5,338,597 (GRCm39) |
V99I |
probably benign |
Het |
Or2w3b |
G |
A |
11: 58,623,271 (GRCm39) |
T240M |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 81,965,479 (GRCm39) |
S549P |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,410,323 (GRCm39) |
F2610S |
probably damaging |
Het |
S100a14 |
A |
G |
3: 90,435,114 (GRCm39) |
T42A |
possibly damaging |
Het |
Serpina6 |
T |
A |
12: 103,613,187 (GRCm39) |
Y371F |
probably benign |
Het |
Slc43a3 |
T |
C |
2: 84,778,782 (GRCm39) |
|
probably benign |
Het |
Taldo1 |
C |
A |
7: 140,972,217 (GRCm39) |
T28K |
probably damaging |
Het |
Tatdn3 |
T |
C |
1: 190,785,097 (GRCm39) |
Y184C |
probably damaging |
Het |
Tep1 |
G |
C |
14: 51,091,667 (GRCm39) |
R625G |
probably benign |
Het |
Timm44 |
A |
T |
8: 4,317,871 (GRCm39) |
I179N |
possibly damaging |
Het |
Uimc1 |
A |
T |
13: 55,198,552 (GRCm39) |
|
probably null |
Het |
Vmn1r68 |
A |
T |
7: 10,262,089 (GRCm39) |
V3E |
probably damaging |
Het |
Zer1 |
A |
T |
2: 29,991,139 (GRCm39) |
F683L |
probably damaging |
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 |
|
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 |
|