Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
T |
3: 59,651,144 (GRCm39) |
I89F |
possibly damaging |
Het |
Abca13 |
T |
A |
11: 9,478,999 (GRCm39) |
H4282Q |
probably benign |
Het |
Acta2 |
A |
G |
19: 34,222,310 (GRCm39) |
|
probably null |
Het |
Arl10 |
A |
G |
13: 54,723,579 (GRCm39) |
|
probably benign |
Het |
Avpr1a |
A |
G |
10: 122,285,623 (GRCm39) |
Y305C |
probably damaging |
Het |
Bmpr2 |
T |
A |
1: 59,906,603 (GRCm39) |
N565K |
probably damaging |
Het |
Boc |
A |
T |
16: 44,307,115 (GRCm39) |
S1035R |
probably benign |
Het |
Brd10 |
A |
T |
19: 29,694,532 (GRCm39) |
S1654T |
probably benign |
Het |
Ccdc7a |
T |
C |
8: 129,753,170 (GRCm39) |
N187S |
possibly damaging |
Het |
Cntn5 |
C |
T |
9: 9,748,457 (GRCm39) |
E680K |
probably damaging |
Het |
Copa |
T |
A |
1: 171,946,835 (GRCm39) |
Y1014* |
probably null |
Het |
Csmd3 |
A |
G |
15: 47,683,847 (GRCm39) |
S1662P |
probably damaging |
Het |
Cyp2e1 |
T |
C |
7: 140,353,042 (GRCm39) |
F360L |
possibly damaging |
Het |
Efnb3 |
A |
T |
11: 69,447,628 (GRCm39) |
|
probably benign |
Het |
Egf |
A |
T |
3: 129,530,529 (GRCm39) |
L211Q |
probably damaging |
Het |
Eno1 |
G |
A |
4: 150,325,583 (GRCm39) |
R56H |
probably benign |
Het |
Fyb2 |
A |
G |
4: 104,852,975 (GRCm39) |
T552A |
probably damaging |
Het |
Git2 |
G |
A |
5: 114,871,918 (GRCm39) |
|
probably benign |
Het |
Gtf2ird2 |
A |
G |
5: 134,245,752 (GRCm39) |
|
probably null |
Het |
Hyal4 |
A |
T |
6: 24,755,964 (GRCm39) |
I61L |
probably benign |
Het |
Kat14 |
T |
C |
2: 144,217,885 (GRCm39) |
|
probably null |
Het |
Kif13b |
T |
C |
14: 65,025,897 (GRCm39) |
V1418A |
probably benign |
Het |
Lcn12 |
T |
C |
2: 25,383,274 (GRCm39) |
K35E |
probably benign |
Het |
Lyrm7 |
G |
T |
11: 54,741,198 (GRCm39) |
N45K |
possibly damaging |
Het |
Mical2 |
G |
T |
7: 111,996,764 (GRCm39) |
G559V |
probably damaging |
Het |
Mtrr |
A |
T |
13: 68,712,441 (GRCm39) |
C648* |
probably null |
Het |
Muc5b |
C |
A |
7: 141,412,556 (GRCm39) |
S1834* |
probably null |
Het |
Mup16 |
G |
A |
4: 61,436,250 (GRCm39) |
T101M |
probably benign |
Het |
Nags |
A |
T |
11: 102,039,814 (GRCm39) |
I501F |
probably damaging |
Het |
Nbeal1 |
A |
T |
1: 60,317,886 (GRCm39) |
Y672F |
probably damaging |
Het |
Ncapg2 |
A |
G |
12: 116,415,993 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
G |
11: 58,891,365 (GRCm39) |
S7056P |
unknown |
Het |
Or52s1 |
T |
C |
7: 102,861,928 (GRCm39) |
I287T |
probably damaging |
Het |
Pde2a |
C |
A |
7: 101,157,890 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,163,343 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
C |
A |
1: 20,268,395 (GRCm39) |
D3328Y |
probably damaging |
Het |
Plxdc2 |
T |
C |
2: 16,654,935 (GRCm39) |
V178A |
probably damaging |
Het |
Prdx3 |
T |
C |
19: 60,861,556 (GRCm39) |
|
probably benign |
Het |
Prkce |
T |
A |
17: 86,961,983 (GRCm39) |
D694E |
probably damaging |
Het |
Prss1l |
T |
A |
6: 41,374,012 (GRCm39) |
C205S |
probably damaging |
Het |
Ptdss1 |
T |
A |
13: 67,142,058 (GRCm39) |
Y405* |
probably null |
Het |
Rad54l |
A |
T |
4: 115,955,729 (GRCm39) |
W608R |
probably damaging |
Het |
Rassf6 |
G |
T |
5: 90,756,649 (GRCm39) |
|
probably benign |
Het |
Sema5a |
A |
T |
15: 32,673,573 (GRCm39) |
I804F |
probably damaging |
Het |
Slc15a2 |
A |
T |
16: 36,572,267 (GRCm39) |
I668N |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 130,116,288 (GRCm39) |
E1347G |
probably benign |
Het |
Tmco3 |
T |
C |
8: 13,348,205 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,551,996 (GRCm39) |
M31214V |
probably null |
Het |
Uck1 |
G |
A |
2: 32,148,334 (GRCm39) |
R161C |
probably benign |
Het |
Ugt2b5 |
T |
C |
5: 87,276,209 (GRCm39) |
Y355C |
probably damaging |
Het |
Usp48 |
C |
A |
4: 137,383,436 (GRCm39) |
T1031K |
probably damaging |
Het |
Vmn1r202 |
G |
A |
13: 22,685,640 (GRCm39) |
T259I |
probably benign |
Het |
Vmn1r202 |
T |
A |
13: 22,685,500 (GRCm39) |
|
probably benign |
Het |
Vmn2r90 |
T |
C |
17: 17,953,771 (GRCm39) |
I645T |
probably damaging |
Het |
Vps18 |
T |
C |
2: 119,124,132 (GRCm39) |
V353A |
possibly damaging |
Het |
Vwf |
C |
T |
6: 125,576,326 (GRCm39) |
Q469* |
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 |
|
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 |
|