Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730409E04Rik |
A |
G |
4: 126,506,104 (GRCm39) |
K211E |
probably damaging |
Het |
Acot7 |
A |
G |
4: 152,291,285 (GRCm39) |
I84V |
possibly damaging |
Het |
Ankrd44 |
A |
G |
1: 54,867,781 (GRCm39) |
V34A |
probably benign |
Het |
Atp4b |
A |
T |
8: 13,443,489 (GRCm39) |
M63K |
probably damaging |
Het |
Atr |
T |
A |
9: 95,818,516 (GRCm39) |
I2163K |
probably damaging |
Het |
Azgp1 |
A |
T |
5: 137,983,426 (GRCm39) |
R34* |
probably null |
Het |
Ccdc152 |
T |
G |
15: 3,327,603 (GRCm39) |
K58T |
probably damaging |
Het |
Ccdc88b |
T |
A |
19: 6,827,837 (GRCm39) |
Q912L |
probably benign |
Het |
Cdc42ep5 |
T |
A |
7: 4,154,395 (GRCm39) |
H131L |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,844,675 (GRCm39) |
E1595K |
probably damaging |
Het |
Col11a1 |
G |
A |
3: 113,925,290 (GRCm39) |
G41D |
probably damaging |
Het |
Cyp2b23 |
C |
T |
7: 26,385,843 (GRCm39) |
V5I |
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,085,915 (GRCm39) |
V22A |
possibly damaging |
Het |
Ddi1 |
T |
C |
9: 6,266,012 (GRCm39) |
Y119C |
probably benign |
Het |
Dysf |
T |
C |
6: 84,083,923 (GRCm39) |
L785P |
probably damaging |
Het |
Eqtn |
T |
A |
4: 94,816,587 (GRCm39) |
T69S |
possibly damaging |
Het |
F11 |
T |
A |
8: 45,694,617 (GRCm39) |
K581N |
probably damaging |
Het |
Gli2 |
G |
A |
1: 118,782,290 (GRCm39) |
P172S |
probably damaging |
Het |
Gm7579 |
G |
T |
7: 141,765,603 (GRCm39) |
C3F |
unknown |
Het |
Grin2a |
A |
G |
16: 9,481,194 (GRCm39) |
V501A |
possibly damaging |
Het |
Grk4 |
G |
A |
5: 34,831,901 (GRCm39) |
D57N |
probably damaging |
Het |
Gsdma |
A |
T |
11: 98,557,319 (GRCm39) |
D86V |
probably damaging |
Het |
Gsx1 |
A |
G |
5: 147,126,738 (GRCm39) |
E187G |
probably damaging |
Het |
Hdac1-ps |
A |
G |
17: 78,799,537 (GRCm39) |
D176G |
probably damaging |
Het |
Inpp5k |
T |
A |
11: 75,524,307 (GRCm39) |
F75L |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,326,620 (GRCm39) |
V114A |
possibly damaging |
Het |
Izumo3 |
A |
T |
4: 92,032,977 (GRCm39) |
C130S |
probably damaging |
Het |
Mei4 |
G |
A |
9: 81,809,639 (GRCm39) |
E241K |
possibly damaging |
Het |
Mocs2 |
T |
C |
13: 114,961,120 (GRCm39) |
V39A |
probably benign |
Het |
Mroh2b |
G |
A |
15: 4,974,572 (GRCm39) |
R1184H |
probably benign |
Het |
Msh3 |
T |
C |
13: 92,436,783 (GRCm39) |
Q509R |
probably null |
Het |
Mypop |
T |
A |
7: 18,734,918 (GRCm39) |
|
probably benign |
Het |
Ndc1 |
C |
A |
4: 107,225,293 (GRCm39) |
T3K |
probably damaging |
Het |
Nf1 |
A |
C |
11: 79,331,749 (GRCm39) |
M695L |
probably benign |
Het |
Nup50l |
A |
G |
6: 96,141,793 (GRCm39) |
M417T |
probably benign |
Het |
Nutm2 |
C |
A |
13: 50,623,955 (GRCm39) |
D217E |
possibly damaging |
Het |
Or52a20 |
T |
C |
7: 103,365,858 (GRCm39) |
I19T |
probably damaging |
Het |
Or5b122 |
A |
G |
19: 13,562,994 (GRCm39) |
T109A |
probably benign |
Het |
Pde6c |
C |
A |
19: 38,129,940 (GRCm39) |
D283E |
probably damaging |
Het |
Phldb2 |
A |
G |
16: 45,591,142 (GRCm39) |
|
probably benign |
Het |
Pigt |
G |
C |
2: 164,349,419 (GRCm39) |
R574P |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,796,500 (GRCm39) |
I2354T |
possibly damaging |
Het |
Prdm15 |
T |
C |
16: 97,640,506 (GRCm39) |
E27G |
probably damaging |
Het |
Ptpn14 |
A |
G |
1: 189,597,709 (GRCm39) |
I1140V |
probably benign |
Het |
Rdx |
T |
C |
9: 51,974,891 (GRCm39) |
V9A |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,519,071 (GRCm39) |
S258P |
probably damaging |
Het |
Rnf17 |
G |
T |
14: 56,730,822 (GRCm39) |
G1209C |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,335,225 (GRCm39) |
|
probably null |
Het |
Scml2 |
G |
T |
X: 160,014,442 (GRCm39) |
E566D |
possibly damaging |
Het |
Serpinb1b |
T |
A |
13: 33,277,646 (GRCm39) |
V293E |
possibly damaging |
Het |
Serpinb9b |
T |
C |
13: 33,222,112 (GRCm39) |
|
probably null |
Het |
Sez6l |
A |
C |
5: 112,622,915 (GRCm39) |
I212S |
probably damaging |
Het |
Son |
T |
C |
16: 91,454,552 (GRCm39) |
S1100P |
probably damaging |
Het |
Spag9 |
G |
A |
11: 93,939,365 (GRCm39) |
R98H |
probably damaging |
Het |
Spata31e2 |
A |
T |
1: 26,723,511 (GRCm39) |
H556Q |
possibly damaging |
Het |
St3gal5 |
T |
C |
6: 72,119,272 (GRCm39) |
L128P |
probably benign |
Het |
Stra6 |
A |
T |
9: 58,059,166 (GRCm39) |
M510L |
probably benign |
Het |
Stxbp5l |
A |
G |
16: 37,028,473 (GRCm39) |
V530A |
probably benign |
Het |
Tatdn1 |
A |
G |
15: 58,793,039 (GRCm39) |
|
probably benign |
Het |
Tbc1d8 |
A |
G |
1: 39,430,206 (GRCm39) |
S466P |
probably benign |
Het |
Tmem199 |
A |
T |
11: 78,399,152 (GRCm39) |
M175K |
possibly damaging |
Het |
Trmt12 |
A |
G |
15: 58,744,764 (GRCm39) |
E54G |
probably benign |
Het |
Usp37 |
G |
T |
1: 74,532,163 (GRCm39) |
Q77K |
possibly damaging |
Het |
Vezf1 |
A |
G |
11: 87,967,125 (GRCm39) |
I301V |
possibly damaging |
Het |
Vmn1r34 |
T |
G |
6: 66,613,932 (GRCm39) |
M269L |
probably benign |
Het |
Wdr93 |
C |
A |
7: 79,421,257 (GRCm39) |
|
probably null |
Het |
Wnk2 |
T |
C |
13: 49,214,370 (GRCm39) |
D644G |
probably damaging |
Het |
Zc3h13 |
C |
T |
14: 75,574,923 (GRCm39) |
R1591* |
probably null |
Het |
Zfp131 |
G |
A |
13: 120,230,316 (GRCm39) |
L371F |
probably damaging |
Het |
Zfp180 |
T |
A |
7: 23,804,049 (GRCm39) |
V156D |
probably benign |
Het |
Zfp646 |
G |
T |
7: 127,479,359 (GRCm39) |
|
probably null |
Het |
Zscan12 |
C |
A |
13: 21,550,813 (GRCm39) |
T144K |
probably benign |
Het |
|
Other mutations in Myh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Myh8
|
APN |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01020:Myh8
|
APN |
11 |
67,174,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01348:Myh8
|
APN |
11 |
67,188,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01382:Myh8
|
APN |
11 |
67,192,799 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01454:Myh8
|
APN |
11 |
67,174,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Myh8
|
APN |
11 |
67,183,505 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01472:Myh8
|
APN |
11 |
67,179,205 (GRCm39) |
splice site |
probably benign |
|
IGL01473:Myh8
|
APN |
11 |
67,192,651 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01613:Myh8
|
APN |
11 |
67,192,536 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01763:Myh8
|
APN |
11 |
67,177,245 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01828:Myh8
|
APN |
11 |
67,194,652 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01862:Myh8
|
APN |
11 |
67,180,520 (GRCm39) |
nonsense |
probably null |
|
IGL01905:Myh8
|
APN |
11 |
67,175,477 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02280:Myh8
|
APN |
11 |
67,174,198 (GRCm39) |
unclassified |
probably benign |
|
IGL02386:Myh8
|
APN |
11 |
67,185,266 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02449:Myh8
|
APN |
11 |
67,185,440 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02500:Myh8
|
APN |
11 |
67,196,536 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02745:Myh8
|
APN |
11 |
67,188,327 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02799:Myh8
|
APN |
11 |
67,192,418 (GRCm39) |
splice site |
probably benign |
|
IGL03063:Myh8
|
APN |
11 |
67,179,031 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03223:Myh8
|
APN |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03336:Myh8
|
APN |
11 |
67,175,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03338:Myh8
|
APN |
11 |
67,189,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Myh8
|
APN |
11 |
67,194,739 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03392:Myh8
|
APN |
11 |
67,185,244 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB009:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
BB013:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB019:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Myh8
|
UTSW |
11 |
67,180,456 (GRCm39) |
missense |
probably benign |
0.01 |
R0012:Myh8
|
UTSW |
11 |
67,190,847 (GRCm39) |
missense |
probably benign |
0.02 |
R0016:Myh8
|
UTSW |
11 |
67,189,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Myh8
|
UTSW |
11 |
67,189,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Myh8
|
UTSW |
11 |
67,197,090 (GRCm39) |
splice site |
probably benign |
|
R0131:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0131:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0132:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0238:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0393:Myh8
|
UTSW |
11 |
67,196,843 (GRCm39) |
splice site |
probably benign |
|
R0453:Myh8
|
UTSW |
11 |
67,183,731 (GRCm39) |
missense |
probably benign |
0.03 |
R0454:Myh8
|
UTSW |
11 |
67,194,591 (GRCm39) |
nonsense |
probably null |
|
R0466:Myh8
|
UTSW |
11 |
67,189,405 (GRCm39) |
missense |
probably benign |
0.01 |
R0487:Myh8
|
UTSW |
11 |
67,192,837 (GRCm39) |
missense |
probably benign |
|
R0511:Myh8
|
UTSW |
11 |
67,175,333 (GRCm39) |
missense |
probably benign |
0.01 |
R0557:Myh8
|
UTSW |
11 |
67,192,624 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0589:Myh8
|
UTSW |
11 |
67,189,453 (GRCm39) |
missense |
probably benign |
0.00 |
R0658:Myh8
|
UTSW |
11 |
67,175,358 (GRCm39) |
critical splice donor site |
probably null |
|
R0782:Myh8
|
UTSW |
11 |
67,180,580 (GRCm39) |
missense |
probably benign |
0.16 |
R0829:Myh8
|
UTSW |
11 |
67,174,326 (GRCm39) |
unclassified |
probably benign |
|
R0845:Myh8
|
UTSW |
11 |
67,177,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Myh8
|
UTSW |
11 |
67,196,824 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0972:Myh8
|
UTSW |
11 |
67,188,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Myh8
|
UTSW |
11 |
67,187,957 (GRCm39) |
nonsense |
probably null |
|
R1417:Myh8
|
UTSW |
11 |
67,197,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Myh8
|
UTSW |
11 |
67,183,551 (GRCm39) |
missense |
probably benign |
0.23 |
R1497:Myh8
|
UTSW |
11 |
67,180,638 (GRCm39) |
missense |
probably benign |
0.00 |
R1701:Myh8
|
UTSW |
11 |
67,170,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Myh8
|
UTSW |
11 |
67,169,830 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1989:Myh8
|
UTSW |
11 |
67,183,550 (GRCm39) |
missense |
probably benign |
0.00 |
R2010:Myh8
|
UTSW |
11 |
67,187,990 (GRCm39) |
nonsense |
probably null |
|
R2095:Myh8
|
UTSW |
11 |
67,177,050 (GRCm39) |
missense |
probably benign |
0.00 |
R2132:Myh8
|
UTSW |
11 |
67,183,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Myh8
|
UTSW |
11 |
67,185,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R2229:Myh8
|
UTSW |
11 |
67,199,174 (GRCm39) |
missense |
probably damaging |
0.98 |
R2302:Myh8
|
UTSW |
11 |
67,177,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Myh8
|
UTSW |
11 |
67,185,344 (GRCm39) |
missense |
probably benign |
0.03 |
R2429:Myh8
|
UTSW |
11 |
67,194,723 (GRCm39) |
missense |
probably benign |
0.21 |
R2880:Myh8
|
UTSW |
11 |
67,188,090 (GRCm39) |
missense |
probably damaging |
0.97 |
R3692:Myh8
|
UTSW |
11 |
67,192,744 (GRCm39) |
missense |
probably damaging |
0.98 |
R3756:Myh8
|
UTSW |
11 |
67,175,443 (GRCm39) |
unclassified |
probably benign |
|
R3924:Myh8
|
UTSW |
11 |
67,187,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R4172:Myh8
|
UTSW |
11 |
67,183,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R4255:Myh8
|
UTSW |
11 |
67,190,560 (GRCm39) |
missense |
probably benign |
|
R4621:Myh8
|
UTSW |
11 |
67,177,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Myh8
|
UTSW |
11 |
67,177,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Myh8
|
UTSW |
11 |
67,170,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Myh8
|
UTSW |
11 |
67,183,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Myh8
|
UTSW |
11 |
67,196,742 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5119:Myh8
|
UTSW |
11 |
67,189,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Myh8
|
UTSW |
11 |
67,179,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R5229:Myh8
|
UTSW |
11 |
67,175,310 (GRCm39) |
missense |
probably damaging |
0.96 |
R5320:Myh8
|
UTSW |
11 |
67,177,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Myh8
|
UTSW |
11 |
67,192,244 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5523:Myh8
|
UTSW |
11 |
67,196,788 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5540:Myh8
|
UTSW |
11 |
67,177,266 (GRCm39) |
missense |
probably benign |
0.00 |
R5726:Myh8
|
UTSW |
11 |
67,185,392 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5770:Myh8
|
UTSW |
11 |
67,188,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Myh8
|
UTSW |
11 |
67,188,326 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6253:Myh8
|
UTSW |
11 |
67,192,793 (GRCm39) |
missense |
probably benign |
0.06 |
R6318:Myh8
|
UTSW |
11 |
67,190,167 (GRCm39) |
missense |
probably benign |
0.00 |
R6432:Myh8
|
UTSW |
11 |
67,189,405 (GRCm39) |
missense |
probably benign |
0.01 |
R6452:Myh8
|
UTSW |
11 |
67,196,565 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6452:Myh8
|
UTSW |
11 |
67,183,275 (GRCm39) |
missense |
probably benign |
0.27 |
R6512:Myh8
|
UTSW |
11 |
67,180,488 (GRCm39) |
nonsense |
probably null |
|
R6714:Myh8
|
UTSW |
11 |
67,197,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Myh8
|
UTSW |
11 |
67,175,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Myh8
|
UTSW |
11 |
67,179,142 (GRCm39) |
missense |
probably benign |
0.03 |
R7025:Myh8
|
UTSW |
11 |
67,188,365 (GRCm39) |
missense |
probably benign |
0.02 |
R7086:Myh8
|
UTSW |
11 |
67,183,453 (GRCm39) |
splice site |
probably null |
|
R7098:Myh8
|
UTSW |
11 |
67,169,879 (GRCm39) |
missense |
probably benign |
0.03 |
R7498:Myh8
|
UTSW |
11 |
67,174,263 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7716:Myh8
|
UTSW |
11 |
67,189,478 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7765:Myh8
|
UTSW |
11 |
67,194,481 (GRCm39) |
missense |
probably benign |
0.44 |
R7825:Myh8
|
UTSW |
11 |
67,194,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7921:Myh8
|
UTSW |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
R7926:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7932:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
R8003:Myh8
|
UTSW |
11 |
67,190,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Myh8
|
UTSW |
11 |
67,194,502 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8121:Myh8
|
UTSW |
11 |
67,180,647 (GRCm39) |
missense |
probably benign |
0.00 |
R8125:Myh8
|
UTSW |
11 |
67,190,598 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8170:Myh8
|
UTSW |
11 |
67,179,092 (GRCm39) |
missense |
probably benign |
0.30 |
R8277:Myh8
|
UTSW |
11 |
67,183,735 (GRCm39) |
missense |
probably benign |
0.10 |
R8304:Myh8
|
UTSW |
11 |
67,195,162 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8431:Myh8
|
UTSW |
11 |
67,174,440 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8535:Myh8
|
UTSW |
11 |
67,169,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Myh8
|
UTSW |
11 |
67,174,203 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8858:Myh8
|
UTSW |
11 |
67,192,820 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8927:Myh8
|
UTSW |
11 |
67,174,081 (GRCm39) |
missense |
probably benign |
0.10 |
R8928:Myh8
|
UTSW |
11 |
67,174,081 (GRCm39) |
missense |
probably benign |
0.10 |
R9031:Myh8
|
UTSW |
11 |
67,190,141 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9172:Myh8
|
UTSW |
11 |
67,183,260 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9252:Myh8
|
UTSW |
11 |
67,177,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9365:Myh8
|
UTSW |
11 |
67,174,632 (GRCm39) |
missense |
probably benign |
0.42 |
R9468:Myh8
|
UTSW |
11 |
67,197,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
R9565:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
T0722:Myh8
|
UTSW |
11 |
67,195,262 (GRCm39) |
missense |
probably benign |
0.41 |
Z1088:Myh8
|
UTSW |
11 |
67,189,418 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myh8
|
UTSW |
11 |
67,194,500 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myh8
|
UTSW |
11 |
67,199,181 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1177:Myh8
|
UTSW |
11 |
67,192,250 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1187:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1188:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1190:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1191:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
|