Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
G |
T |
7: 29,260,263 (GRCm39) |
|
noncoding transcript |
Het |
Adam21 |
C |
T |
12: 81,606,047 (GRCm39) |
V572I |
probably damaging |
Het |
Arhgap32 |
T |
A |
9: 32,063,315 (GRCm39) |
|
probably null |
Het |
Carmil1 |
A |
T |
13: 24,321,152 (GRCm39) |
I281N |
probably damaging |
Het |
Cdh12 |
T |
A |
15: 21,586,063 (GRCm39) |
|
probably null |
Het |
Cdh20 |
T |
A |
1: 109,976,734 (GRCm39) |
V133E |
probably benign |
Het |
Cntrob |
A |
G |
11: 69,193,708 (GRCm39) |
L814P |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,252,000 (GRCm39) |
N952S |
probably damaging |
Het |
Cspg4 |
A |
G |
9: 56,795,517 (GRCm39) |
Y1084C |
probably damaging |
Het |
Dlg5 |
A |
G |
14: 24,240,378 (GRCm39) |
|
probably benign |
Het |
Glis2 |
T |
C |
16: 4,431,760 (GRCm39) |
|
probably benign |
Het |
Hif3a |
T |
C |
7: 16,788,638 (GRCm39) |
E111G |
probably damaging |
Het |
Kctd4 |
A |
G |
14: 76,200,251 (GRCm39) |
D74G |
probably benign |
Het |
Kif21b |
A |
T |
1: 136,083,964 (GRCm39) |
K737M |
probably damaging |
Het |
Ktn1 |
G |
A |
14: 47,943,860 (GRCm39) |
|
probably benign |
Het |
Lama2 |
A |
T |
10: 27,335,335 (GRCm39) |
N113K |
probably damaging |
Het |
Ltv1 |
A |
G |
10: 13,054,944 (GRCm39) |
S409P |
probably benign |
Het |
Mgat4c |
A |
G |
10: 102,224,782 (GRCm39) |
E332G |
probably benign |
Het |
Ndufa4l2 |
A |
G |
10: 127,351,289 (GRCm39) |
I27V |
probably benign |
Het |
Npepl1 |
T |
G |
2: 173,962,447 (GRCm39) |
L371R |
probably damaging |
Het |
Nudt9 |
A |
G |
5: 104,194,972 (GRCm39) |
T23A |
probably benign |
Het |
Ocrl |
G |
A |
X: 47,027,180 (GRCm39) |
V416I |
probably benign |
Het |
Or2g1 |
T |
G |
17: 38,106,895 (GRCm39) |
C187G |
probably damaging |
Het |
Padi2 |
C |
T |
4: 140,645,048 (GRCm39) |
T94I |
probably benign |
Het |
Pcca |
G |
A |
14: 122,922,297 (GRCm39) |
E353K |
probably damaging |
Het |
Pcdhgb2 |
T |
A |
18: 37,824,810 (GRCm39) |
N600K |
probably damaging |
Het |
Pex5l |
A |
G |
3: 33,004,993 (GRCm39) |
L593P |
probably damaging |
Het |
Rbp2 |
G |
A |
9: 98,380,879 (GRCm39) |
D62N |
probably benign |
Het |
Rock1 |
G |
T |
18: 10,067,575 (GRCm39) |
N1319K |
probably benign |
Het |
Ror1 |
A |
C |
4: 100,269,314 (GRCm39) |
D384A |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Sacm1l |
A |
T |
9: 123,381,855 (GRCm39) |
E152D |
probably benign |
Het |
Seh1l |
T |
C |
18: 67,908,087 (GRCm39) |
V3A |
probably benign |
Het |
Serpinb6d |
T |
A |
13: 33,848,097 (GRCm39) |
D20E |
probably benign |
Het |
Serpini1 |
T |
G |
3: 75,521,942 (GRCm39) |
N144K |
probably damaging |
Het |
Slc22a23 |
G |
A |
13: 34,528,323 (GRCm39) |
T153I |
probably benign |
Het |
Slfn8 |
A |
G |
11: 82,908,280 (GRCm39) |
S88P |
probably benign |
Het |
Stpg3 |
T |
A |
2: 25,103,875 (GRCm39) |
M154L |
probably benign |
Het |
Vmn2r115 |
G |
A |
17: 23,564,146 (GRCm39) |
C106Y |
probably damaging |
Het |
Washc3 |
C |
T |
10: 88,055,122 (GRCm39) |
T112M |
probably benign |
Het |
Zfp280d |
C |
T |
9: 72,229,806 (GRCm39) |
T346M |
probably damaging |
Het |
|
Other mutations in Myh6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Myh6
|
APN |
14 |
55,184,450 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00401:Myh6
|
APN |
14 |
55,190,874 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01062:Myh6
|
APN |
14 |
55,189,749 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01300:Myh6
|
APN |
14 |
55,200,548 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01688:Myh6
|
APN |
14 |
55,201,417 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL01695:Myh6
|
APN |
14 |
55,194,870 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01762:Myh6
|
APN |
14 |
55,199,538 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01803:Myh6
|
APN |
14 |
55,182,000 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02079:Myh6
|
APN |
14 |
55,187,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02315:Myh6
|
APN |
14 |
55,191,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Myh6
|
APN |
14 |
55,194,612 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02377:Myh6
|
APN |
14 |
55,181,775 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02715:Myh6
|
APN |
14 |
55,184,365 (GRCm39) |
unclassified |
probably benign |
|
IGL02742:Myh6
|
APN |
14 |
55,191,381 (GRCm39) |
missense |
possibly damaging |
0.62 |
P0028:Myh6
|
UTSW |
14 |
55,201,094 (GRCm39) |
missense |
probably benign |
|
PIT4520001:Myh6
|
UTSW |
14 |
55,187,581 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Myh6
|
UTSW |
14 |
55,200,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Myh6
|
UTSW |
14 |
55,196,161 (GRCm39) |
missense |
probably damaging |
0.97 |
R0360:Myh6
|
UTSW |
14 |
55,185,804 (GRCm39) |
nonsense |
probably null |
|
R0364:Myh6
|
UTSW |
14 |
55,185,804 (GRCm39) |
nonsense |
probably null |
|
R0395:Myh6
|
UTSW |
14 |
55,183,777 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0549:Myh6
|
UTSW |
14 |
55,196,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R0559:Myh6
|
UTSW |
14 |
55,196,011 (GRCm39) |
missense |
probably benign |
|
R0800:Myh6
|
UTSW |
14 |
55,190,735 (GRCm39) |
splice site |
probably benign |
|
R0892:Myh6
|
UTSW |
14 |
55,184,511 (GRCm39) |
missense |
probably benign |
0.17 |
R0975:Myh6
|
UTSW |
14 |
55,190,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Myh6
|
UTSW |
14 |
55,186,984 (GRCm39) |
missense |
probably benign |
0.12 |
R1180:Myh6
|
UTSW |
14 |
55,181,925 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1311:Myh6
|
UTSW |
14 |
55,183,822 (GRCm39) |
missense |
probably damaging |
0.96 |
R1490:Myh6
|
UTSW |
14 |
55,200,175 (GRCm39) |
nonsense |
probably null |
|
R1531:Myh6
|
UTSW |
14 |
55,193,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Myh6
|
UTSW |
14 |
55,194,858 (GRCm39) |
missense |
probably benign |
0.03 |
R1845:Myh6
|
UTSW |
14 |
55,182,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R2033:Myh6
|
UTSW |
14 |
55,201,102 (GRCm39) |
missense |
probably benign |
0.00 |
R2143:Myh6
|
UTSW |
14 |
55,190,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R2146:Myh6
|
UTSW |
14 |
55,191,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R2155:Myh6
|
UTSW |
14 |
55,191,251 (GRCm39) |
missense |
probably benign |
|
R2484:Myh6
|
UTSW |
14 |
55,198,699 (GRCm39) |
nonsense |
probably null |
|
R3155:Myh6
|
UTSW |
14 |
55,182,125 (GRCm39) |
missense |
probably damaging |
0.97 |
R3156:Myh6
|
UTSW |
14 |
55,182,125 (GRCm39) |
missense |
probably damaging |
0.97 |
R3906:Myh6
|
UTSW |
14 |
55,194,412 (GRCm39) |
missense |
probably benign |
0.04 |
R3937:Myh6
|
UTSW |
14 |
55,200,512 (GRCm39) |
missense |
probably benign |
0.00 |
R3938:Myh6
|
UTSW |
14 |
55,200,512 (GRCm39) |
missense |
probably benign |
0.00 |
R4236:Myh6
|
UTSW |
14 |
55,197,819 (GRCm39) |
missense |
probably benign |
0.15 |
R4373:Myh6
|
UTSW |
14 |
55,199,565 (GRCm39) |
missense |
probably damaging |
0.97 |
R4374:Myh6
|
UTSW |
14 |
55,199,565 (GRCm39) |
missense |
probably damaging |
0.97 |
R4377:Myh6
|
UTSW |
14 |
55,199,565 (GRCm39) |
missense |
probably damaging |
0.97 |
R4798:Myh6
|
UTSW |
14 |
55,190,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Myh6
|
UTSW |
14 |
55,184,651 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4908:Myh6
|
UTSW |
14 |
55,194,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Myh6
|
UTSW |
14 |
55,190,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Myh6
|
UTSW |
14 |
55,194,019 (GRCm39) |
missense |
probably benign |
0.01 |
R5356:Myh6
|
UTSW |
14 |
55,191,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Myh6
|
UTSW |
14 |
55,191,381 (GRCm39) |
missense |
probably benign |
0.32 |
R5616:Myh6
|
UTSW |
14 |
55,194,038 (GRCm39) |
missense |
probably benign |
0.17 |
R5784:Myh6
|
UTSW |
14 |
55,190,521 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5820:Myh6
|
UTSW |
14 |
55,196,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R5835:Myh6
|
UTSW |
14 |
55,187,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R5922:Myh6
|
UTSW |
14 |
55,183,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R5975:Myh6
|
UTSW |
14 |
55,187,965 (GRCm39) |
missense |
probably benign |
0.31 |
R5988:Myh6
|
UTSW |
14 |
55,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R6630:Myh6
|
UTSW |
14 |
55,179,458 (GRCm39) |
missense |
probably benign |
0.01 |
R6845:Myh6
|
UTSW |
14 |
55,182,206 (GRCm39) |
missense |
probably benign |
|
R7009:Myh6
|
UTSW |
14 |
55,189,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R7154:Myh6
|
UTSW |
14 |
55,197,764 (GRCm39) |
missense |
probably benign |
0.43 |
R7293:Myh6
|
UTSW |
14 |
55,184,631 (GRCm39) |
missense |
probably benign |
0.00 |
R7313:Myh6
|
UTSW |
14 |
55,197,727 (GRCm39) |
missense |
probably benign |
0.00 |
R7339:Myh6
|
UTSW |
14 |
55,199,025 (GRCm39) |
splice site |
probably null |
|
R7348:Myh6
|
UTSW |
14 |
55,189,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R7487:Myh6
|
UTSW |
14 |
55,190,953 (GRCm39) |
nonsense |
probably null |
|
R7680:Myh6
|
UTSW |
14 |
55,186,190 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7726:Myh6
|
UTSW |
14 |
55,202,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R7743:Myh6
|
UTSW |
14 |
55,194,607 (GRCm39) |
missense |
probably damaging |
0.99 |
R7807:Myh6
|
UTSW |
14 |
55,179,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R7851:Myh6
|
UTSW |
14 |
55,190,508 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8145:Myh6
|
UTSW |
14 |
55,191,382 (GRCm39) |
missense |
probably benign |
0.45 |
R8344:Myh6
|
UTSW |
14 |
55,190,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R8407:Myh6
|
UTSW |
14 |
55,201,388 (GRCm39) |
missense |
probably benign |
0.13 |
R8415:Myh6
|
UTSW |
14 |
55,181,835 (GRCm39) |
missense |
probably damaging |
0.98 |
R8782:Myh6
|
UTSW |
14 |
55,187,357 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9034:Myh6
|
UTSW |
14 |
55,185,596 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9354:Myh6
|
UTSW |
14 |
55,200,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R9441:Myh6
|
UTSW |
14 |
55,197,771 (GRCm39) |
missense |
probably benign |
0.02 |
R9449:Myh6
|
UTSW |
14 |
55,189,779 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9485:Myh6
|
UTSW |
14 |
55,181,802 (GRCm39) |
missense |
probably benign |
0.01 |
R9612:Myh6
|
UTSW |
14 |
55,201,054 (GRCm39) |
missense |
probably benign |
0.09 |
R9738:Myh6
|
UTSW |
14 |
55,189,759 (GRCm39) |
missense |
probably benign |
0.03 |
R9742:Myh6
|
UTSW |
14 |
55,194,056 (GRCm39) |
missense |
probably benign |
|
R9749:Myh6
|
UTSW |
14 |
55,190,943 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Myh6
|
UTSW |
14 |
55,194,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|