Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adrb3 |
T |
C |
8: 27,716,880 (GRCm39) |
|
probably benign |
Het |
Atg2b |
T |
C |
12: 105,602,767 (GRCm39) |
H1592R |
probably benign |
Het |
Bpifb1 |
C |
T |
2: 154,044,581 (GRCm39) |
A16V |
probably benign |
Het |
Cep57 |
T |
A |
9: 13,721,166 (GRCm39) |
Y271F |
probably damaging |
Het |
Cfap54 |
A |
T |
10: 92,803,397 (GRCm39) |
N1548K |
possibly damaging |
Het |
Chrna6 |
A |
T |
8: 27,898,408 (GRCm39) |
D103E |
probably benign |
Het |
Clec12b |
T |
C |
6: 129,357,651 (GRCm39) |
N69S |
probably benign |
Het |
Col27a1 |
T |
C |
4: 63,209,815 (GRCm39) |
|
probably null |
Het |
Cwh43 |
T |
A |
5: 73,565,526 (GRCm39) |
Y30* |
probably null |
Het |
Dnai7 |
A |
G |
6: 145,127,483 (GRCm39) |
|
probably null |
Het |
Dsg4 |
T |
C |
18: 20,582,429 (GRCm39) |
|
probably null |
Het |
Efna3 |
T |
C |
3: 89,223,880 (GRCm39) |
N103S |
probably damaging |
Het |
Efr3a |
A |
G |
15: 65,725,400 (GRCm39) |
D532G |
possibly damaging |
Het |
Fam227a |
A |
T |
15: 79,510,469 (GRCm39) |
V395D |
probably benign |
Het |
Fes |
T |
A |
7: 80,036,668 (GRCm39) |
D93V |
probably damaging |
Het |
Gbp3 |
T |
A |
3: 142,276,732 (GRCm39) |
M510K |
possibly damaging |
Het |
Gpr12 |
A |
T |
5: 146,520,314 (GRCm39) |
S44T |
probably damaging |
Het |
Gpr179 |
T |
C |
11: 97,234,100 (GRCm39) |
N583S |
probably damaging |
Het |
Hipk1 |
T |
C |
3: 103,651,620 (GRCm39) |
T1093A |
probably benign |
Het |
Hspb1 |
T |
C |
5: 135,918,097 (GRCm39) |
L148P |
probably damaging |
Het |
Kirrel3 |
A |
G |
9: 34,946,161 (GRCm39) |
N640S |
probably damaging |
Het |
Mak |
G |
T |
13: 41,199,545 (GRCm39) |
Q365K |
probably benign |
Het |
Melk |
A |
G |
4: 44,303,649 (GRCm39) |
Y14C |
unknown |
Het |
Nsmf |
A |
G |
2: 24,950,522 (GRCm39) |
Y330C |
probably damaging |
Het |
Parp14 |
A |
G |
16: 35,661,172 (GRCm39) |
F1592S |
possibly damaging |
Het |
Pnpla6 |
A |
T |
8: 3,573,317 (GRCm39) |
I394F |
probably benign |
Het |
Ppl |
T |
C |
16: 4,906,918 (GRCm39) |
R1126G |
probably damaging |
Het |
Prss8 |
C |
T |
7: 127,525,646 (GRCm39) |
R291Q |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rasgrp1 |
G |
T |
2: 117,130,980 (GRCm39) |
D155E |
probably benign |
Het |
Recql5 |
T |
C |
11: 115,786,628 (GRCm39) |
I563V |
probably benign |
Het |
Rhbg |
C |
T |
3: 88,151,875 (GRCm39) |
M394I |
probably benign |
Het |
Rnf130 |
A |
G |
11: 49,978,264 (GRCm39) |
D275G |
probably damaging |
Het |
Smg9 |
T |
C |
7: 24,120,289 (GRCm39) |
F421S |
probably benign |
Het |
Tgm2 |
T |
C |
2: 157,966,301 (GRCm39) |
E451G |
probably damaging |
Het |
Tle1 |
T |
A |
4: 72,117,598 (GRCm39) |
T21S |
probably damaging |
Het |
Tmc5 |
T |
C |
7: 118,226,433 (GRCm39) |
I266T |
possibly damaging |
Het |
Tmigd3 |
T |
A |
3: 105,824,318 (GRCm39) |
C96S |
probably damaging |
Het |
Trdn |
A |
T |
10: 33,181,077 (GRCm39) |
T361S |
probably benign |
Het |
Vgll3 |
A |
T |
16: 65,657,568 (GRCm39) |
Q261L |
probably benign |
Het |
Vmn2r104 |
A |
T |
17: 20,262,987 (GRCm39) |
I158K |
probably benign |
Het |
Zfp964 |
A |
G |
8: 70,116,731 (GRCm39) |
K444E |
possibly damaging |
Het |
|
Other mutations in Myh7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Myh7
|
APN |
14 |
55,224,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01025:Myh7
|
APN |
14 |
55,216,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01092:Myh7
|
APN |
14 |
55,209,089 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01384:Myh7
|
APN |
14 |
55,208,916 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Myh7
|
APN |
14 |
55,226,336 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01671:Myh7
|
APN |
14 |
55,210,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Myh7
|
APN |
14 |
55,222,916 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02183:Myh7
|
APN |
14 |
55,212,188 (GRCm39) |
missense |
probably benign |
|
IGL02379:Myh7
|
APN |
14 |
55,216,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Myh7
|
APN |
14 |
55,230,276 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02898:Myh7
|
APN |
14 |
55,221,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Myh7
|
APN |
14 |
55,221,007 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Myh7
|
APN |
14 |
55,228,661 (GRCm39) |
unclassified |
probably benign |
|
IGL03145:Myh7
|
APN |
14 |
55,220,802 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03250:Myh7
|
APN |
14 |
55,229,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03394:Myh7
|
APN |
14 |
55,212,818 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
BB018:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0019:Myh7
|
UTSW |
14 |
55,221,191 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0030:Myh7
|
UTSW |
14 |
55,229,427 (GRCm39) |
missense |
probably benign |
0.00 |
R0183:Myh7
|
UTSW |
14 |
55,216,333 (GRCm39) |
missense |
probably benign |
0.02 |
R0230:Myh7
|
UTSW |
14 |
55,211,390 (GRCm39) |
missense |
probably benign |
0.03 |
R0295:Myh7
|
UTSW |
14 |
55,222,278 (GRCm39) |
splice site |
probably benign |
|
R0423:Myh7
|
UTSW |
14 |
55,216,646 (GRCm39) |
missense |
probably benign |
0.06 |
R0537:Myh7
|
UTSW |
14 |
55,228,256 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0541:Myh7
|
UTSW |
14 |
55,212,158 (GRCm39) |
missense |
probably benign |
|
R0581:Myh7
|
UTSW |
14 |
55,222,953 (GRCm39) |
missense |
probably benign |
0.02 |
R0866:Myh7
|
UTSW |
14 |
55,210,596 (GRCm39) |
missense |
probably benign |
|
R1068:Myh7
|
UTSW |
14 |
55,224,776 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1075:Myh7
|
UTSW |
14 |
55,224,860 (GRCm39) |
missense |
probably benign |
|
R1124:Myh7
|
UTSW |
14 |
55,211,327 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1140:Myh7
|
UTSW |
14 |
55,210,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Myh7
|
UTSW |
14 |
55,225,908 (GRCm39) |
missense |
probably benign |
0.00 |
R1653:Myh7
|
UTSW |
14 |
55,228,246 (GRCm39) |
missense |
probably benign |
0.00 |
R1677:Myh7
|
UTSW |
14 |
55,224,973 (GRCm39) |
missense |
probably benign |
0.17 |
R1760:Myh7
|
UTSW |
14 |
55,210,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Myh7
|
UTSW |
14 |
55,210,637 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1839:Myh7
|
UTSW |
14 |
55,210,637 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2483:Myh7
|
UTSW |
14 |
55,210,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R2566:Myh7
|
UTSW |
14 |
55,220,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Myh7
|
UTSW |
14 |
55,210,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R3916:Myh7
|
UTSW |
14 |
55,211,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R4236:Myh7
|
UTSW |
14 |
55,228,575 (GRCm39) |
missense |
probably benign |
0.34 |
R4471:Myh7
|
UTSW |
14 |
55,229,311 (GRCm39) |
nonsense |
probably null |
|
R4700:Myh7
|
UTSW |
14 |
55,225,778 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4805:Myh7
|
UTSW |
14 |
55,222,590 (GRCm39) |
missense |
probably benign |
0.27 |
R4880:Myh7
|
UTSW |
14 |
55,216,045 (GRCm39) |
missense |
probably benign |
0.18 |
R4975:Myh7
|
UTSW |
14 |
55,209,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Myh7
|
UTSW |
14 |
55,210,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R5004:Myh7
|
UTSW |
14 |
55,209,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R5107:Myh7
|
UTSW |
14 |
55,223,881 (GRCm39) |
intron |
probably benign |
|
R5124:Myh7
|
UTSW |
14 |
55,223,199 (GRCm39) |
nonsense |
probably null |
|
R5256:Myh7
|
UTSW |
14 |
55,216,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Myh7
|
UTSW |
14 |
55,224,020 (GRCm39) |
intron |
probably benign |
|
R5581:Myh7
|
UTSW |
14 |
55,216,411 (GRCm39) |
missense |
probably benign |
0.00 |
R5861:Myh7
|
UTSW |
14 |
55,226,347 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5957:Myh7
|
UTSW |
14 |
55,226,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Myh7
|
UTSW |
14 |
55,208,259 (GRCm39) |
missense |
probably benign |
0.01 |
R6184:Myh7
|
UTSW |
14 |
55,226,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Myh7
|
UTSW |
14 |
55,226,753 (GRCm39) |
missense |
probably benign |
0.00 |
R6268:Myh7
|
UTSW |
14 |
55,226,741 (GRCm39) |
missense |
probably benign |
0.00 |
R6274:Myh7
|
UTSW |
14 |
55,216,943 (GRCm39) |
missense |
probably damaging |
0.97 |
R6345:Myh7
|
UTSW |
14 |
55,221,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Myh7
|
UTSW |
14 |
55,226,351 (GRCm39) |
missense |
probably benign |
0.00 |
R6641:Myh7
|
UTSW |
14 |
55,219,737 (GRCm39) |
missense |
probably benign |
0.37 |
R6755:Myh7
|
UTSW |
14 |
55,229,770 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6952:Myh7
|
UTSW |
14 |
55,229,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Myh7
|
UTSW |
14 |
55,212,101 (GRCm39) |
nonsense |
probably null |
|
R7201:Myh7
|
UTSW |
14 |
55,228,402 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7257:Myh7
|
UTSW |
14 |
55,209,947 (GRCm39) |
splice site |
probably null |
|
R7296:Myh7
|
UTSW |
14 |
55,227,482 (GRCm39) |
missense |
probably benign |
0.05 |
R7709:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Myh7
|
UTSW |
14 |
55,227,500 (GRCm39) |
missense |
probably benign |
0.09 |
R7869:Myh7
|
UTSW |
14 |
55,226,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7931:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7936:Myh7
|
UTSW |
14 |
55,216,920 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8056:Myh7
|
UTSW |
14 |
55,210,776 (GRCm39) |
nonsense |
probably null |
|
R8061:Myh7
|
UTSW |
14 |
55,228,398 (GRCm39) |
missense |
probably benign |
|
R8101:Myh7
|
UTSW |
14 |
55,210,776 (GRCm39) |
nonsense |
probably null |
|
R8202:Myh7
|
UTSW |
14 |
55,227,497 (GRCm39) |
missense |
probably benign |
|
R8504:Myh7
|
UTSW |
14 |
55,227,786 (GRCm39) |
missense |
probably damaging |
0.98 |
R8560:Myh7
|
UTSW |
14 |
55,213,405 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8843:Myh7
|
UTSW |
14 |
55,212,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R8903:Myh7
|
UTSW |
14 |
55,230,228 (GRCm39) |
nonsense |
probably null |
|
R8926:Myh7
|
UTSW |
14 |
55,222,533 (GRCm39) |
missense |
probably benign |
0.33 |
R8936:Myh7
|
UTSW |
14 |
55,228,440 (GRCm39) |
missense |
probably benign |
0.00 |
R9182:Myh7
|
UTSW |
14 |
55,226,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Myh7
|
UTSW |
14 |
55,224,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R9264:Myh7
|
UTSW |
14 |
55,213,454 (GRCm39) |
missense |
probably benign |
0.01 |
R9288:Myh7
|
UTSW |
14 |
55,222,932 (GRCm39) |
missense |
probably benign |
0.35 |
R9362:Myh7
|
UTSW |
14 |
55,222,932 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Myh7
|
UTSW |
14 |
55,217,841 (GRCm39) |
missense |
probably benign |
0.12 |
R9561:Myh7
|
UTSW |
14 |
55,216,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Myh7
|
UTSW |
14 |
55,221,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R9789:Myh7
|
UTSW |
14 |
55,229,384 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1192:Myh7
|
UTSW |
14 |
55,220,748 (GRCm39) |
missense |
probably damaging |
0.99 |
|