Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam5 |
A |
T |
8: 25,296,502 (GRCm39) |
V315D |
probably damaging |
Het |
Adgrf1 |
A |
T |
17: 43,621,286 (GRCm39) |
I508F |
probably damaging |
Het |
Atpaf2 |
T |
C |
11: 60,298,129 (GRCm39) |
D147G |
probably damaging |
Het |
Brwd1 |
T |
C |
16: 95,817,409 (GRCm39) |
T1368A |
probably damaging |
Het |
Cacna1s |
A |
T |
1: 136,043,799 (GRCm39) |
E1626V |
probably benign |
Het |
Carm1 |
G |
A |
9: 21,480,765 (GRCm39) |
V80I |
possibly damaging |
Het |
Cenpw |
T |
A |
10: 30,074,484 (GRCm39) |
D71V |
probably damaging |
Het |
Cit |
T |
A |
5: 116,122,603 (GRCm39) |
|
probably null |
Het |
Ckmt1 |
A |
T |
2: 121,193,531 (GRCm39) |
T364S |
probably benign |
Het |
Col6a4 |
T |
C |
9: 105,945,583 (GRCm39) |
S844G |
probably benign |
Het |
Crybg1 |
T |
C |
10: 43,868,538 (GRCm39) |
E1380G |
probably benign |
Het |
Cyp21a1 |
A |
G |
17: 35,021,105 (GRCm39) |
|
probably null |
Het |
Dhodh |
A |
C |
8: 110,333,038 (GRCm39) |
D12E |
probably benign |
Het |
Dnali1 |
T |
A |
4: 124,957,460 (GRCm39) |
T95S |
probably damaging |
Het |
Dynlrb1 |
A |
G |
2: 155,091,870 (GRCm39) |
N93D |
probably benign |
Het |
Edem1 |
C |
T |
6: 108,823,774 (GRCm39) |
A390V |
probably benign |
Het |
Enthd1 |
T |
C |
15: 80,358,356 (GRCm39) |
D388G |
probably benign |
Het |
Fam170a |
A |
G |
18: 50,414,677 (GRCm39) |
T108A |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,233,276 (GRCm39) |
S1531P |
probably benign |
Het |
Golm2 |
A |
T |
2: 121,697,632 (GRCm39) |
|
probably benign |
Het |
Hspbap1 |
C |
A |
16: 35,645,366 (GRCm39) |
N350K |
probably benign |
Het |
Htr3b |
A |
C |
9: 48,858,596 (GRCm39) |
S94R |
probably damaging |
Het |
Ide |
A |
T |
19: 37,307,886 (GRCm39) |
V42E |
|
Het |
Igf2r |
A |
G |
17: 12,902,748 (GRCm39) |
V2434A |
probably benign |
Het |
Katnip |
T |
C |
7: 125,468,023 (GRCm39) |
|
probably null |
Het |
Kif16b |
G |
A |
2: 142,553,777 (GRCm39) |
A1007V |
probably benign |
Het |
Mccc1 |
C |
T |
3: 36,018,493 (GRCm39) |
V614I |
probably benign |
Het |
Mos |
A |
G |
4: 3,871,097 (GRCm39) |
Y240H |
probably damaging |
Het |
Nexn |
T |
A |
3: 151,953,998 (GRCm39) |
D166V |
probably damaging |
Het |
Or10h1b |
G |
A |
17: 33,395,895 (GRCm39) |
C173Y |
probably damaging |
Het |
Or2t47 |
G |
T |
11: 58,443,029 (GRCm39) |
T12N |
probably benign |
Het |
Or4p4 |
A |
T |
2: 88,483,332 (GRCm39) |
M279L |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,267,518 (GRCm39) |
N298K |
probably benign |
Het |
Pkp4 |
A |
G |
2: 59,180,895 (GRCm39) |
Y1061C |
probably damaging |
Het |
Pla2g6 |
T |
C |
15: 79,171,370 (GRCm39) |
D740G |
probably damaging |
Het |
Pla2r1 |
T |
A |
2: 60,273,627 (GRCm39) |
I920L |
probably benign |
Het |
Plekha2 |
A |
G |
8: 25,578,407 (GRCm39) |
I31T |
probably damaging |
Het |
Ppp1r16b |
G |
T |
2: 158,603,295 (GRCm39) |
V407L |
probably benign |
Het |
Prss50 |
A |
G |
9: 110,691,370 (GRCm39) |
I225V |
probably damaging |
Het |
Rmdn2 |
A |
T |
17: 79,935,580 (GRCm39) |
E231V |
|
Het |
Sema3c |
T |
C |
5: 17,858,726 (GRCm39) |
S42P |
possibly damaging |
Het |
Sh2d1b1 |
T |
A |
1: 170,110,693 (GRCm39) |
|
probably null |
Het |
Slc22a20 |
T |
C |
19: 6,021,554 (GRCm39) |
I483V |
probably benign |
Het |
Slc30a2 |
T |
C |
4: 134,076,690 (GRCm39) |
V275A |
probably damaging |
Het |
Slc6a3 |
T |
A |
13: 73,693,002 (GRCm39) |
F207L |
probably benign |
Het |
Slc9a1 |
A |
T |
4: 133,147,927 (GRCm39) |
Q648H |
probably damaging |
Het |
Slpi |
A |
T |
2: 164,197,975 (GRCm39) |
M1K |
probably null |
Het |
Smc5 |
A |
C |
19: 23,211,443 (GRCm39) |
S564A |
possibly damaging |
Het |
Smchd1 |
A |
T |
17: 71,738,238 (GRCm39) |
F542L |
probably damaging |
Het |
Sycp1 |
T |
A |
3: 102,727,909 (GRCm39) |
K901N |
probably damaging |
Het |
Synpo2l |
T |
A |
14: 20,716,208 (GRCm39) |
T126S |
probably benign |
Het |
Upp2 |
A |
G |
2: 58,667,955 (GRCm39) |
N216S |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,969,408 (GRCm39) |
D349G |
probably damaging |
Het |
Zfp180 |
C |
T |
7: 23,804,337 (GRCm39) |
A252V |
probably benign |
Het |
Zfr2 |
C |
T |
10: 81,078,653 (GRCm39) |
T295I |
possibly damaging |
Het |
Zkscan16 |
C |
T |
4: 58,957,230 (GRCm39) |
T504I |
possibly damaging |
Het |
|
Other mutations in Myh11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01362:Myh11
|
APN |
16 |
14,095,586 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01398:Myh11
|
APN |
16 |
14,019,964 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01646:Myh11
|
APN |
16 |
14,039,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02470:Myh11
|
APN |
16 |
14,035,910 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02680:Myh11
|
APN |
16 |
14,027,384 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02687:Myh11
|
APN |
16 |
14,030,482 (GRCm39) |
nonsense |
probably null |
|
IGL02987:Myh11
|
APN |
16 |
14,050,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Myh11
|
APN |
16 |
14,022,617 (GRCm39) |
missense |
probably benign |
0.00 |
G5030:Myh11
|
UTSW |
16 |
14,068,443 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4618001:Myh11
|
UTSW |
16 |
14,018,930 (GRCm39) |
missense |
|
|
R0008:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0085:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0086:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Myh11
|
UTSW |
16 |
14,022,231 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0096:Myh11
|
UTSW |
16 |
14,022,231 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0207:Myh11
|
UTSW |
16 |
14,029,124 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0326:Myh11
|
UTSW |
16 |
14,036,744 (GRCm39) |
missense |
probably benign |
0.32 |
R0546:Myh11
|
UTSW |
16 |
14,023,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0715:Myh11
|
UTSW |
16 |
14,044,480 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0839:Myh11
|
UTSW |
16 |
14,021,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R1014:Myh11
|
UTSW |
16 |
14,054,274 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1104:Myh11
|
UTSW |
16 |
14,019,991 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1426:Myh11
|
UTSW |
16 |
14,023,795 (GRCm39) |
nonsense |
probably null |
|
R1560:Myh11
|
UTSW |
16 |
14,044,484 (GRCm39) |
nonsense |
probably null |
|
R1714:Myh11
|
UTSW |
16 |
14,054,232 (GRCm39) |
critical splice donor site |
probably null |
|
R1742:Myh11
|
UTSW |
16 |
14,037,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Myh11
|
UTSW |
16 |
14,033,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R1750:Myh11
|
UTSW |
16 |
14,018,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Myh11
|
UTSW |
16 |
14,095,734 (GRCm39) |
missense |
probably benign |
|
R1760:Myh11
|
UTSW |
16 |
14,051,559 (GRCm39) |
splice site |
probably benign |
|
R1829:Myh11
|
UTSW |
16 |
14,041,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Myh11
|
UTSW |
16 |
14,086,967 (GRCm39) |
splice site |
probably benign |
|
R2027:Myh11
|
UTSW |
16 |
14,050,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Myh11
|
UTSW |
16 |
14,035,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R2247:Myh11
|
UTSW |
16 |
14,095,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2495:Myh11
|
UTSW |
16 |
14,023,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R2863:Myh11
|
UTSW |
16 |
14,057,290 (GRCm39) |
missense |
probably benign |
0.02 |
R3684:Myh11
|
UTSW |
16 |
14,021,098 (GRCm39) |
missense |
probably benign |
0.00 |
R3693:Myh11
|
UTSW |
16 |
14,035,813 (GRCm39) |
missense |
probably benign |
0.01 |
R4080:Myh11
|
UTSW |
16 |
14,041,923 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4367:Myh11
|
UTSW |
16 |
14,036,747 (GRCm39) |
missense |
probably damaging |
0.97 |
R4664:Myh11
|
UTSW |
16 |
14,044,448 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4673:Myh11
|
UTSW |
16 |
14,087,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R4694:Myh11
|
UTSW |
16 |
14,018,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4805:Myh11
|
UTSW |
16 |
14,052,329 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4806:Myh11
|
UTSW |
16 |
14,018,947 (GRCm39) |
splice site |
probably null |
|
R4905:Myh11
|
UTSW |
16 |
14,068,387 (GRCm39) |
missense |
probably benign |
0.13 |
R4939:Myh11
|
UTSW |
16 |
14,057,371 (GRCm39) |
missense |
probably benign |
|
R4964:Myh11
|
UTSW |
16 |
14,023,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4966:Myh11
|
UTSW |
16 |
14,023,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5029:Myh11
|
UTSW |
16 |
14,023,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Myh11
|
UTSW |
16 |
14,057,391 (GRCm39) |
nonsense |
probably null |
|
R5097:Myh11
|
UTSW |
16 |
14,023,770 (GRCm39) |
splice site |
probably null |
|
R5288:Myh11
|
UTSW |
16 |
14,025,872 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5385:Myh11
|
UTSW |
16 |
14,025,872 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5621:Myh11
|
UTSW |
16 |
14,062,719 (GRCm39) |
missense |
probably damaging |
0.96 |
R5856:Myh11
|
UTSW |
16 |
14,023,840 (GRCm39) |
missense |
probably benign |
0.00 |
R5869:Myh11
|
UTSW |
16 |
14,048,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Myh11
|
UTSW |
16 |
14,023,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6024:Myh11
|
UTSW |
16 |
14,095,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R6139:Myh11
|
UTSW |
16 |
14,033,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Myh11
|
UTSW |
16 |
14,026,155 (GRCm39) |
nonsense |
probably null |
|
R6373:Myh11
|
UTSW |
16 |
14,022,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6671:Myh11
|
UTSW |
16 |
14,044,480 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6688:Myh11
|
UTSW |
16 |
14,023,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R6709:Myh11
|
UTSW |
16 |
14,041,358 (GRCm39) |
critical splice donor site |
probably null |
|
R7069:Myh11
|
UTSW |
16 |
14,036,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7176:Myh11
|
UTSW |
16 |
14,033,690 (GRCm39) |
missense |
|
|
R7644:Myh11
|
UTSW |
16 |
14,039,688 (GRCm39) |
missense |
|
|
R7838:Myh11
|
UTSW |
16 |
14,027,481 (GRCm39) |
missense |
|
|
R7905:Myh11
|
UTSW |
16 |
14,025,545 (GRCm39) |
nonsense |
probably null |
|
R8261:Myh11
|
UTSW |
16 |
14,041,867 (GRCm39) |
missense |
|
|
R8272:Myh11
|
UTSW |
16 |
14,036,718 (GRCm39) |
missense |
|
|
R8317:Myh11
|
UTSW |
16 |
14,025,941 (GRCm39) |
missense |
|
|
R8486:Myh11
|
UTSW |
16 |
14,022,532 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8527:Myh11
|
UTSW |
16 |
14,048,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R8861:Myh11
|
UTSW |
16 |
14,064,646 (GRCm39) |
missense |
|
|
R8886:Myh11
|
UTSW |
16 |
14,052,278 (GRCm39) |
missense |
|
|
R8946:Myh11
|
UTSW |
16 |
14,048,580 (GRCm39) |
missense |
probably benign |
0.08 |
R9151:Myh11
|
UTSW |
16 |
14,050,439 (GRCm39) |
missense |
|
|
R9253:Myh11
|
UTSW |
16 |
14,074,359 (GRCm39) |
missense |
|
|
R9257:Myh11
|
UTSW |
16 |
14,087,120 (GRCm39) |
missense |
|
|
R9273:Myh11
|
UTSW |
16 |
14,054,283 (GRCm39) |
missense |
|
|
R9320:Myh11
|
UTSW |
16 |
14,029,152 (GRCm39) |
missense |
|
|
R9364:Myh11
|
UTSW |
16 |
14,018,580 (GRCm39) |
missense |
|
|
R9365:Myh11
|
UTSW |
16 |
14,052,297 (GRCm39) |
missense |
|
|
R9496:Myh11
|
UTSW |
16 |
14,048,616 (GRCm39) |
nonsense |
probably null |
|
R9499:Myh11
|
UTSW |
16 |
14,064,673 (GRCm39) |
missense |
|
|
R9551:Myh11
|
UTSW |
16 |
14,064,673 (GRCm39) |
missense |
|
|
R9554:Myh11
|
UTSW |
16 |
14,018,580 (GRCm39) |
missense |
|
|
R9631:Myh11
|
UTSW |
16 |
14,025,441 (GRCm39) |
missense |
|
|
R9661:Myh11
|
UTSW |
16 |
14,041,857 (GRCm39) |
missense |
|
|
R9679:Myh11
|
UTSW |
16 |
14,095,436 (GRCm39) |
missense |
|
|
R9780:Myh11
|
UTSW |
16 |
14,064,613 (GRCm39) |
missense |
|
|
R9790:Myh11
|
UTSW |
16 |
14,025,992 (GRCm39) |
missense |
|
|
R9791:Myh11
|
UTSW |
16 |
14,025,992 (GRCm39) |
missense |
|
|
X0018:Myh11
|
UTSW |
16 |
14,095,497 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Myh11
|
UTSW |
16 |
14,027,553 (GRCm39) |
missense |
possibly damaging |
0.93 |
X0027:Myh11
|
UTSW |
16 |
14,052,266 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Myh11
|
UTSW |
16 |
14,087,126 (GRCm39) |
frame shift |
probably null |
|
Z1176:Myh11
|
UTSW |
16 |
14,095,639 (GRCm39) |
missense |
|
|
Z1176:Myh11
|
UTSW |
16 |
14,057,260 (GRCm39) |
missense |
probably null |
|
Z1177:Myh11
|
UTSW |
16 |
14,027,459 (GRCm39) |
missense |
|
|
|