Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl1 |
A |
T |
7: 76,418,722 (GRCm38) |
E93D |
possibly damaging |
Het |
Akap10 |
C |
A |
11: 61,915,501 (GRCm38) |
V134F |
possibly damaging |
Het |
Bnc1 |
T |
C |
7: 81,974,073 (GRCm38) |
I469V |
possibly damaging |
Het |
Bod1l |
T |
A |
5: 41,821,545 (GRCm38) |
I809L |
possibly damaging |
Het |
Dicer1 |
T |
A |
12: 104,730,188 (GRCm38) |
E118V |
probably damaging |
Het |
Dmbt1 |
T |
C |
7: 131,046,562 (GRCm38) |
F274S |
probably benign |
Het |
Dnaaf2 |
T |
G |
12: 69,196,644 (GRCm38) |
T548P |
possibly damaging |
Het |
Dysf |
G |
A |
6: 84,186,509 (GRCm38) |
|
probably null |
Het |
Fchsd2 |
A |
G |
7: 101,233,885 (GRCm38) |
N240S |
probably benign |
Het |
Foxb1 |
T |
C |
9: 69,759,864 (GRCm38) |
Y128C |
probably damaging |
Het |
Fxr2 |
A |
T |
11: 69,642,070 (GRCm38) |
K158M |
possibly damaging |
Het |
Gm438 |
G |
A |
4: 144,777,421 (GRCm38) |
R387C |
probably benign |
Het |
Golga4 |
C |
A |
9: 118,556,904 (GRCm38) |
D1031E |
probably benign |
Het |
Hbb-bs |
T |
C |
7: 103,827,811 (GRCm38) |
D22G |
possibly damaging |
Het |
Hivep2 |
C |
A |
10: 14,128,969 (GRCm38) |
T437K |
probably benign |
Het |
Hnrnpul2 |
T |
A |
19: 8,820,637 (GRCm38) |
M119K |
probably benign |
Het |
Kif18a |
C |
A |
2: 109,298,107 (GRCm38) |
H369Q |
probably damaging |
Het |
Klhdc10 |
A |
G |
6: 30,449,559 (GRCm38) |
T207A |
probably damaging |
Het |
Lig4 |
A |
G |
8: 9,972,161 (GRCm38) |
C540R |
possibly damaging |
Het |
Lilr4b |
A |
T |
10: 51,481,608 (GRCm38) |
N133Y |
possibly damaging |
Het |
Lrrc31 |
T |
A |
3: 30,685,030 (GRCm38) |
|
probably benign |
Het |
Mslnl |
G |
A |
17: 25,742,934 (GRCm38) |
V128M |
probably damaging |
Het |
Nlrp2 |
C |
T |
7: 5,335,598 (GRCm38) |
V99I |
probably benign |
Het |
Olfr317 |
G |
A |
11: 58,732,445 (GRCm38) |
T240M |
probably damaging |
Het |
Pcnx |
T |
C |
12: 81,918,705 (GRCm38) |
S549P |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,546,927 (GRCm38) |
F2610S |
probably damaging |
Het |
S100a14 |
A |
G |
3: 90,527,807 (GRCm38) |
T42A |
possibly damaging |
Het |
Serpina6 |
T |
A |
12: 103,646,928 (GRCm38) |
Y371F |
probably benign |
Het |
Slc43a3 |
T |
C |
2: 84,948,438 (GRCm38) |
|
probably benign |
Het |
Taldo1 |
C |
A |
7: 141,392,304 (GRCm38) |
T28K |
probably damaging |
Het |
Tatdn3 |
T |
C |
1: 191,052,900 (GRCm38) |
Y184C |
probably damaging |
Het |
Tep1 |
G |
C |
14: 50,854,210 (GRCm38) |
R625G |
probably benign |
Het |
Timm44 |
A |
T |
8: 4,267,871 (GRCm38) |
I179N |
possibly damaging |
Het |
Uimc1 |
A |
T |
13: 55,050,739 (GRCm38) |
|
probably null |
Het |
Vmn1r68 |
A |
T |
7: 10,528,162 (GRCm38) |
V3E |
probably damaging |
Het |
Zer1 |
A |
T |
2: 30,101,127 (GRCm38) |
F683L |
probably damaging |
Het |
|
Other mutations in Myof |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Myof
|
APN |
19 |
37,960,934 (GRCm38) |
missense |
probably benign |
0.16 |
IGL00764:Myof
|
APN |
19 |
37,974,923 (GRCm38) |
missense |
probably benign |
0.04 |
IGL00801:Myof
|
APN |
19 |
37,986,073 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01084:Myof
|
APN |
19 |
37,936,436 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01368:Myof
|
APN |
19 |
37,936,457 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01472:Myof
|
APN |
19 |
37,923,076 (GRCm38) |
missense |
probably benign |
|
IGL01785:Myof
|
APN |
19 |
37,980,423 (GRCm38) |
nonsense |
probably null |
|
IGL02205:Myof
|
APN |
19 |
37,924,635 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02268:Myof
|
APN |
19 |
37,974,863 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL02268:Myof
|
APN |
19 |
37,954,429 (GRCm38) |
missense |
possibly damaging |
0.50 |
IGL02339:Myof
|
APN |
19 |
37,972,213 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02433:Myof
|
APN |
19 |
37,972,193 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02481:Myof
|
APN |
19 |
37,937,913 (GRCm38) |
nonsense |
probably null |
|
IGL02536:Myof
|
APN |
19 |
37,949,655 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02682:Myof
|
APN |
19 |
37,921,481 (GRCm38) |
missense |
probably benign |
0.09 |
IGL02732:Myof
|
APN |
19 |
37,977,716 (GRCm38) |
missense |
possibly damaging |
0.50 |
IGL02887:Myof
|
APN |
19 |
37,920,779 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL03114:Myof
|
APN |
19 |
37,903,861 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03137:Myof
|
APN |
19 |
37,974,889 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03340:Myof
|
APN |
19 |
37,911,159 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4791001:Myof
|
UTSW |
19 |
37,982,958 (GRCm38) |
critical splice donor site |
probably null |
|
R0024:Myof
|
UTSW |
19 |
37,915,740 (GRCm38) |
missense |
probably damaging |
0.98 |
R0140:Myof
|
UTSW |
19 |
37,951,556 (GRCm38) |
nonsense |
probably null |
|
R0309:Myof
|
UTSW |
19 |
37,981,266 (GRCm38) |
missense |
probably benign |
0.12 |
R0330:Myof
|
UTSW |
19 |
37,935,878 (GRCm38) |
missense |
probably damaging |
1.00 |
R0345:Myof
|
UTSW |
19 |
38,024,345 (GRCm38) |
missense |
probably damaging |
1.00 |
R0349:Myof
|
UTSW |
19 |
37,910,969 (GRCm38) |
missense |
probably damaging |
0.99 |
R0463:Myof
|
UTSW |
19 |
37,916,504 (GRCm38) |
missense |
probably damaging |
1.00 |
R0507:Myof
|
UTSW |
19 |
37,901,277 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0512:Myof
|
UTSW |
19 |
37,954,524 (GRCm38) |
missense |
possibly damaging |
0.54 |
R0608:Myof
|
UTSW |
19 |
37,916,504 (GRCm38) |
missense |
probably damaging |
1.00 |
R0723:Myof
|
UTSW |
19 |
37,981,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R1081:Myof
|
UTSW |
19 |
37,986,088 (GRCm38) |
missense |
probably damaging |
0.99 |
R1196:Myof
|
UTSW |
19 |
37,910,960 (GRCm38) |
missense |
probably damaging |
1.00 |
R1243:Myof
|
UTSW |
19 |
37,936,092 (GRCm38) |
missense |
probably damaging |
1.00 |
R1371:Myof
|
UTSW |
19 |
37,903,668 (GRCm38) |
splice site |
probably benign |
|
R1381:Myof
|
UTSW |
19 |
37,995,485 (GRCm38) |
missense |
probably damaging |
1.00 |
R1419:Myof
|
UTSW |
19 |
37,901,911 (GRCm38) |
missense |
probably damaging |
1.00 |
R1527:Myof
|
UTSW |
19 |
37,924,619 (GRCm38) |
missense |
probably damaging |
1.00 |
R1672:Myof
|
UTSW |
19 |
37,943,479 (GRCm38) |
missense |
probably damaging |
1.00 |
R1864:Myof
|
UTSW |
19 |
37,986,705 (GRCm38) |
missense |
probably benign |
|
R1914:Myof
|
UTSW |
19 |
37,977,693 (GRCm38) |
missense |
probably damaging |
1.00 |
R1915:Myof
|
UTSW |
19 |
37,977,693 (GRCm38) |
missense |
probably damaging |
1.00 |
R1970:Myof
|
UTSW |
19 |
37,945,634 (GRCm38) |
missense |
probably damaging |
0.99 |
R2062:Myof
|
UTSW |
19 |
37,915,746 (GRCm38) |
missense |
possibly damaging |
0.94 |
R2144:Myof
|
UTSW |
19 |
37,981,221 (GRCm38) |
critical splice donor site |
probably null |
|
R2339:Myof
|
UTSW |
19 |
37,937,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R2484:Myof
|
UTSW |
19 |
37,903,843 (GRCm38) |
missense |
probably benign |
0.13 |
R2880:Myof
|
UTSW |
19 |
37,923,025 (GRCm38) |
missense |
probably benign |
0.04 |
R3418:Myof
|
UTSW |
19 |
37,922,978 (GRCm38) |
missense |
probably damaging |
0.97 |
R3967:Myof
|
UTSW |
19 |
38,022,610 (GRCm38) |
missense |
possibly damaging |
0.59 |
R3967:Myof
|
UTSW |
19 |
37,901,263 (GRCm38) |
missense |
probably damaging |
1.00 |
R3970:Myof
|
UTSW |
19 |
38,022,610 (GRCm38) |
missense |
possibly damaging |
0.59 |
R3970:Myof
|
UTSW |
19 |
37,901,263 (GRCm38) |
missense |
probably damaging |
1.00 |
R4238:Myof
|
UTSW |
19 |
37,923,008 (GRCm38) |
nonsense |
probably null |
|
R4405:Myof
|
UTSW |
19 |
37,922,978 (GRCm38) |
missense |
probably damaging |
0.97 |
R4406:Myof
|
UTSW |
19 |
37,922,978 (GRCm38) |
missense |
probably damaging |
0.97 |
R4407:Myof
|
UTSW |
19 |
37,922,978 (GRCm38) |
missense |
probably damaging |
0.97 |
R4408:Myof
|
UTSW |
19 |
37,922,978 (GRCm38) |
missense |
probably damaging |
0.97 |
R4561:Myof
|
UTSW |
19 |
37,922,990 (GRCm38) |
missense |
probably benign |
|
R4606:Myof
|
UTSW |
19 |
37,967,099 (GRCm38) |
missense |
probably damaging |
1.00 |
R4778:Myof
|
UTSW |
19 |
37,949,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R4801:Myof
|
UTSW |
19 |
37,945,738 (GRCm38) |
missense |
probably benign |
0.24 |
R4802:Myof
|
UTSW |
19 |
37,945,738 (GRCm38) |
missense |
probably benign |
0.24 |
R4812:Myof
|
UTSW |
19 |
37,916,559 (GRCm38) |
missense |
probably damaging |
1.00 |
R4884:Myof
|
UTSW |
19 |
37,942,357 (GRCm38) |
missense |
probably damaging |
1.00 |
R4964:Myof
|
UTSW |
19 |
37,935,852 (GRCm38) |
missense |
probably damaging |
0.97 |
R4966:Myof
|
UTSW |
19 |
37,935,852 (GRCm38) |
missense |
probably damaging |
0.97 |
R5069:Myof
|
UTSW |
19 |
37,905,325 (GRCm38) |
missense |
possibly damaging |
0.65 |
R5181:Myof
|
UTSW |
19 |
37,932,623 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5376:Myof
|
UTSW |
19 |
37,916,400 (GRCm38) |
missense |
probably damaging |
1.00 |
R5384:Myof
|
UTSW |
19 |
37,952,987 (GRCm38) |
missense |
probably damaging |
0.98 |
R5543:Myof
|
UTSW |
19 |
37,981,330 (GRCm38) |
missense |
probably benign |
0.00 |
R5626:Myof
|
UTSW |
19 |
37,922,990 (GRCm38) |
missense |
probably benign |
|
R5865:Myof
|
UTSW |
19 |
37,910,934 (GRCm38) |
missense |
probably damaging |
1.00 |
R5919:Myof
|
UTSW |
19 |
38,024,370 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5924:Myof
|
UTSW |
19 |
37,982,973 (GRCm38) |
missense |
probably damaging |
0.97 |
R5997:Myof
|
UTSW |
19 |
37,905,299 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5999:Myof
|
UTSW |
19 |
37,939,856 (GRCm38) |
nonsense |
probably null |
|
R6039:Myof
|
UTSW |
19 |
37,977,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R6039:Myof
|
UTSW |
19 |
37,977,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R6041:Myof
|
UTSW |
19 |
37,924,620 (GRCm38) |
missense |
probably damaging |
1.00 |
R6051:Myof
|
UTSW |
19 |
38,024,361 (GRCm38) |
missense |
probably damaging |
1.00 |
R6057:Myof
|
UTSW |
19 |
37,926,981 (GRCm38) |
critical splice donor site |
probably null |
|
R6089:Myof
|
UTSW |
19 |
37,967,060 (GRCm38) |
missense |
probably benign |
0.37 |
R6195:Myof
|
UTSW |
19 |
37,913,357 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6478:Myof
|
UTSW |
19 |
37,903,831 (GRCm38) |
missense |
probably damaging |
1.00 |
R6545:Myof
|
UTSW |
19 |
37,942,297 (GRCm38) |
missense |
possibly damaging |
0.67 |
R6655:Myof
|
UTSW |
19 |
37,934,791 (GRCm38) |
missense |
probably damaging |
1.00 |
R6715:Myof
|
UTSW |
19 |
37,968,346 (GRCm38) |
missense |
probably benign |
0.04 |
R6737:Myof
|
UTSW |
19 |
37,943,514 (GRCm38) |
missense |
probably benign |
0.01 |
R6837:Myof
|
UTSW |
19 |
37,922,956 (GRCm38) |
critical splice donor site |
probably null |
|
R7096:Myof
|
UTSW |
19 |
37,936,200 (GRCm38) |
missense |
probably damaging |
1.00 |
R7308:Myof
|
UTSW |
19 |
37,910,911 (GRCm38) |
missense |
probably damaging |
0.98 |
R7328:Myof
|
UTSW |
19 |
37,916,399 (GRCm38) |
missense |
probably damaging |
1.00 |
R7485:Myof
|
UTSW |
19 |
37,951,491 (GRCm38) |
nonsense |
probably null |
|
R7554:Myof
|
UTSW |
19 |
37,954,510 (GRCm38) |
missense |
probably benign |
0.09 |
R7759:Myof
|
UTSW |
19 |
37,939,898 (GRCm38) |
missense |
probably benign |
0.00 |
R7779:Myof
|
UTSW |
19 |
37,939,390 (GRCm38) |
missense |
probably damaging |
1.00 |
R8116:Myof
|
UTSW |
19 |
37,932,719 (GRCm38) |
missense |
probably damaging |
0.99 |
R8264:Myof
|
UTSW |
19 |
37,921,433 (GRCm38) |
missense |
probably damaging |
1.00 |
R8415:Myof
|
UTSW |
19 |
37,995,424 (GRCm38) |
missense |
probably benign |
|
R8756:Myof
|
UTSW |
19 |
37,939,952 (GRCm38) |
missense |
probably benign |
|
R8777:Myof
|
UTSW |
19 |
37,980,393 (GRCm38) |
missense |
probably benign |
0.01 |
R8777-TAIL:Myof
|
UTSW |
19 |
37,980,393 (GRCm38) |
missense |
probably benign |
0.01 |
R8835:Myof
|
UTSW |
19 |
37,967,099 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9046:Myof
|
UTSW |
19 |
37,934,664 (GRCm38) |
intron |
probably benign |
|
R9396:Myof
|
UTSW |
19 |
37,934,846 (GRCm38) |
missense |
probably damaging |
1.00 |
R9415:Myof
|
UTSW |
19 |
37,952,964 (GRCm38) |
missense |
probably damaging |
1.00 |
R9450:Myof
|
UTSW |
19 |
37,960,926 (GRCm38) |
missense |
probably damaging |
1.00 |
R9451:Myof
|
UTSW |
19 |
37,977,648 (GRCm38) |
critical splice donor site |
probably null |
|
R9537:Myof
|
UTSW |
19 |
37,907,606 (GRCm38) |
missense |
probably damaging |
1.00 |
R9592:Myof
|
UTSW |
19 |
38,043,289 (GRCm38) |
missense |
probably damaging |
0.99 |
R9616:Myof
|
UTSW |
19 |
37,934,815 (GRCm38) |
missense |
possibly damaging |
0.52 |
R9751:Myof
|
UTSW |
19 |
37,936,370 (GRCm38) |
missense |
probably benign |
|
X0024:Myof
|
UTSW |
19 |
37,974,597 (GRCm38) |
missense |
probably benign |
0.14 |
|