Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
A |
G |
8: 60,979,656 (GRCm39) |
I173V |
probably benign |
Het |
Abi3bp |
C |
T |
16: 56,382,734 (GRCm39) |
R115C |
probably damaging |
Het |
Adam18 |
A |
G |
8: 25,141,868 (GRCm39) |
S234P |
possibly damaging |
Het |
Adam20 |
A |
G |
8: 41,249,449 (GRCm39) |
R520G |
probably benign |
Het |
Angel2 |
C |
G |
1: 190,677,194 (GRCm39) |
T514R |
probably damaging |
Het |
Ankar |
A |
T |
1: 72,698,192 (GRCm39) |
I954N |
probably benign |
Het |
Ankrd7 |
A |
T |
6: 18,879,342 (GRCm39) |
Y262F |
probably benign |
Het |
Ano8 |
C |
A |
8: 71,935,007 (GRCm39) |
L398F |
possibly damaging |
Het |
App |
C |
T |
16: 84,822,319 (GRCm39) |
V356I |
probably benign |
Het |
Atp1a2 |
C |
A |
1: 172,108,194 (GRCm39) |
E636* |
probably null |
Het |
Cckbr |
G |
A |
7: 105,084,552 (GRCm39) |
E429K |
possibly damaging |
Het |
Cfi |
T |
G |
3: 129,648,708 (GRCm39) |
S197R |
probably damaging |
Het |
Chn2 |
A |
G |
6: 54,263,162 (GRCm39) |
|
probably null |
Het |
Col3a1 |
C |
A |
1: 45,370,860 (GRCm39) |
A405D |
unknown |
Het |
Colec12 |
A |
T |
18: 9,848,248 (GRCm39) |
N142I |
probably benign |
Het |
Copa |
T |
C |
1: 171,947,511 (GRCm39) |
L1109P |
probably damaging |
Het |
Cpeb3 |
T |
A |
19: 37,152,152 (GRCm39) |
M75L |
probably benign |
Het |
Cyp2d11 |
T |
C |
15: 82,275,969 (GRCm39) |
Y204C |
probably benign |
Het |
Defa17 |
A |
G |
8: 22,146,613 (GRCm39) |
T80A |
probably benign |
Het |
Dnaaf9 |
C |
A |
2: 130,648,708 (GRCm39) |
R258L |
unknown |
Het |
Dppa5a |
C |
T |
9: 78,275,002 (GRCm39) |
|
probably null |
Het |
Fat4 |
G |
T |
3: 38,943,033 (GRCm39) |
S642I |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,038,044 (GRCm39) |
C3899S |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,641,482 (GRCm39) |
V1869A |
probably damaging |
Het |
Gm10308 |
A |
T |
17: 91,396,389 (GRCm39) |
I104L |
unknown |
Het |
Gpr139 |
C |
T |
7: 118,743,896 (GRCm39) |
A230T |
possibly damaging |
Het |
Grm8 |
T |
C |
6: 27,618,486 (GRCm39) |
N452S |
probably benign |
Het |
Hmox1 |
T |
C |
8: 75,823,551 (GRCm39) |
V73A |
probably benign |
Het |
Hspa4 |
A |
G |
11: 53,156,765 (GRCm39) |
F641L |
probably damaging |
Het |
Ifi207 |
T |
G |
1: 173,557,490 (GRCm39) |
H416P |
possibly damaging |
Het |
Igkv10-96 |
G |
T |
6: 68,609,028 (GRCm39) |
T89K |
possibly damaging |
Het |
Kmt2d |
A |
C |
15: 98,741,714 (GRCm39) |
V4482G |
unknown |
Het |
Krt28 |
T |
A |
11: 99,265,230 (GRCm39) |
K146* |
probably null |
Het |
Krt82 |
T |
C |
15: 101,451,191 (GRCm39) |
N406S |
probably damaging |
Het |
Marveld3 |
A |
T |
8: 110,686,477 (GRCm39) |
|
probably null |
Het |
Mllt6 |
C |
T |
11: 97,564,394 (GRCm39) |
S370L |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,585,750 (GRCm39) |
L26S |
unknown |
Het |
Mup12 |
T |
A |
4: 60,696,734 (GRCm39) |
E48V |
probably benign |
Het |
Nipal3 |
G |
A |
4: 135,201,732 (GRCm39) |
T152I |
probably benign |
Het |
Nrg3 |
A |
T |
14: 39,194,435 (GRCm39) |
M108K |
probably benign |
Het |
Nup50l |
T |
G |
6: 96,141,756 (GRCm39) |
E429D |
probably benign |
Het |
Oog3 |
A |
T |
4: 143,889,169 (GRCm39) |
I3N |
probably damaging |
Het |
Or10d4c |
G |
A |
9: 39,558,387 (GRCm39) |
V122I |
probably benign |
Het |
Pira13 |
A |
G |
7: 3,827,792 (GRCm39) |
W122R |
|
Het |
Pkhd1l1 |
T |
C |
15: 44,392,512 (GRCm39) |
C1616R |
probably damaging |
Het |
Ppa2 |
T |
A |
3: 133,053,953 (GRCm39) |
|
probably null |
Het |
Ppfibp2 |
T |
A |
7: 107,322,187 (GRCm39) |
|
probably null |
Het |
Ppp4c |
T |
C |
7: 126,385,653 (GRCm39) |
N229D |
probably damaging |
Het |
Ptpn9 |
T |
C |
9: 56,929,570 (GRCm39) |
F96L |
probably damaging |
Het |
Pygl |
A |
G |
12: 70,241,094 (GRCm39) |
V742A |
probably benign |
Het |
Ranbp2 |
A |
G |
10: 58,312,591 (GRCm39) |
T1104A |
probably benign |
Het |
Rasal1 |
G |
A |
5: 120,813,557 (GRCm39) |
A644T |
probably benign |
Het |
Rcor3 |
T |
A |
1: 191,810,261 (GRCm39) |
T139S |
possibly damaging |
Het |
Rfx5 |
T |
A |
3: 94,862,454 (GRCm39) |
I37N |
probably damaging |
Het |
Rnf112 |
C |
T |
11: 61,341,683 (GRCm39) |
G374R |
probably damaging |
Het |
Rrp12 |
T |
C |
19: 41,859,979 (GRCm39) |
I1034V |
probably benign |
Het |
Sacs |
T |
A |
14: 61,447,538 (GRCm39) |
Y3195N |
possibly damaging |
Het |
Scn4a |
A |
G |
11: 106,215,062 (GRCm39) |
I1243T |
probably benign |
Het |
Sirt7 |
A |
T |
11: 120,509,799 (GRCm39) |
C362S |
probably benign |
Het |
Slc17a6 |
T |
A |
7: 51,276,640 (GRCm39) |
S130T |
probably damaging |
Het |
Snrnp48 |
A |
C |
13: 38,393,875 (GRCm39) |
Y60S |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,060,859 (GRCm39) |
E7260G |
probably damaging |
Het |
Trbv15 |
C |
T |
6: 41,118,529 (GRCm39) |
T95I |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,771,943 (GRCm39) |
N68K |
probably benign |
Het |
Ugcg |
A |
G |
4: 59,213,210 (GRCm39) |
Y132C |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,304,672 (GRCm39) |
C2391S |
probably damaging |
Het |
Vmn1r103 |
C |
A |
7: 20,244,438 (GRCm39) |
V8L |
probably benign |
Het |
Vmn2r15 |
T |
A |
5: 109,440,649 (GRCm39) |
N403I |
probably damaging |
Het |
Zbtb11 |
T |
C |
16: 55,827,551 (GRCm39) |
S1006P |
probably damaging |
Het |
|
Other mutations in Myh1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Myh1
|
APN |
11 |
67,111,691 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00514:Myh1
|
APN |
11 |
67,110,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00851:Myh1
|
APN |
11 |
67,108,736 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01061:Myh1
|
APN |
11 |
67,108,688 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01113:Myh1
|
APN |
11 |
67,093,006 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01125:Myh1
|
APN |
11 |
67,111,486 (GRCm39) |
missense |
probably benign |
|
IGL01391:Myh1
|
APN |
11 |
67,108,689 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01392:Myh1
|
APN |
11 |
67,112,127 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01404:Myh1
|
APN |
11 |
67,112,977 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01700:Myh1
|
APN |
11 |
67,102,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01739:Myh1
|
APN |
11 |
67,105,354 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01759:Myh1
|
APN |
11 |
67,110,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01922:Myh1
|
APN |
11 |
67,101,292 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01952:Myh1
|
APN |
11 |
67,111,218 (GRCm39) |
splice site |
probably null |
|
IGL02007:Myh1
|
APN |
11 |
67,111,382 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02028:Myh1
|
APN |
11 |
67,101,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02245:Myh1
|
APN |
11 |
67,102,313 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02628:Myh1
|
APN |
11 |
67,097,088 (GRCm39) |
unclassified |
probably benign |
|
IGL02942:Myh1
|
APN |
11 |
67,093,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Myh1
|
APN |
11 |
67,099,896 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03031:Myh1
|
APN |
11 |
67,097,213 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03187:Myh1
|
APN |
11 |
67,097,351 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL03302:Myh1
|
APN |
11 |
67,102,328 (GRCm39) |
missense |
probably benign |
0.01 |
compelling
|
UTSW |
11 |
67,110,631 (GRCm39) |
critical splice donor site |
probably null |
|
convincing
|
UTSW |
11 |
67,093,365 (GRCm39) |
missense |
probably damaging |
1.00 |
muscle
|
UTSW |
11 |
67,096,874 (GRCm39) |
nonsense |
probably null |
|
Persuasive
|
UTSW |
11 |
67,099,890 (GRCm39) |
missense |
possibly damaging |
0.90 |
G1patch:Myh1
|
UTSW |
11 |
67,092,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Myh1
|
UTSW |
11 |
67,099,904 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0079:Myh1
|
UTSW |
11 |
67,104,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Myh1
|
UTSW |
11 |
67,106,683 (GRCm39) |
missense |
probably benign |
|
R0317:Myh1
|
UTSW |
11 |
67,108,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0465:Myh1
|
UTSW |
11 |
67,101,243 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0528:Myh1
|
UTSW |
11 |
67,111,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Myh1
|
UTSW |
11 |
67,093,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R0964:Myh1
|
UTSW |
11 |
67,096,751 (GRCm39) |
missense |
probably benign |
|
R0964:Myh1
|
UTSW |
11 |
67,112,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1427:Myh1
|
UTSW |
11 |
67,110,573 (GRCm39) |
missense |
probably damaging |
0.99 |
R1429:Myh1
|
UTSW |
11 |
67,108,736 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1481:Myh1
|
UTSW |
11 |
67,096,325 (GRCm39) |
unclassified |
probably benign |
|
R1562:Myh1
|
UTSW |
11 |
67,102,196 (GRCm39) |
missense |
probably benign |
0.04 |
R1727:Myh1
|
UTSW |
11 |
67,101,292 (GRCm39) |
critical splice donor site |
probably benign |
|
R1796:Myh1
|
UTSW |
11 |
67,115,183 (GRCm39) |
missense |
probably benign |
0.00 |
R1808:Myh1
|
UTSW |
11 |
67,102,300 (GRCm39) |
nonsense |
probably null |
|
R1836:Myh1
|
UTSW |
11 |
67,095,648 (GRCm39) |
missense |
probably damaging |
0.98 |
R1848:Myh1
|
UTSW |
11 |
67,104,456 (GRCm39) |
missense |
probably benign |
0.10 |
R1851:Myh1
|
UTSW |
11 |
67,095,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Myh1
|
UTSW |
11 |
67,101,996 (GRCm39) |
missense |
probably benign |
0.01 |
R1967:Myh1
|
UTSW |
11 |
67,104,273 (GRCm39) |
missense |
probably benign |
0.08 |
R1999:Myh1
|
UTSW |
11 |
67,113,234 (GRCm39) |
missense |
probably benign |
0.04 |
R2067:Myh1
|
UTSW |
11 |
67,105,446 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2111:Myh1
|
UTSW |
11 |
67,105,446 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2150:Myh1
|
UTSW |
11 |
67,113,234 (GRCm39) |
missense |
probably benign |
0.04 |
R2189:Myh1
|
UTSW |
11 |
67,112,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2352:Myh1
|
UTSW |
11 |
67,111,363 (GRCm39) |
missense |
probably benign |
0.00 |
R2436:Myh1
|
UTSW |
11 |
67,104,097 (GRCm39) |
missense |
probably benign |
0.04 |
R2483:Myh1
|
UTSW |
11 |
67,102,052 (GRCm39) |
missense |
probably benign |
|
R2508:Myh1
|
UTSW |
11 |
67,104,424 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2509:Myh1
|
UTSW |
11 |
67,096,423 (GRCm39) |
missense |
probably benign |
0.01 |
R2511:Myh1
|
UTSW |
11 |
67,096,423 (GRCm39) |
missense |
probably benign |
0.01 |
R2908:Myh1
|
UTSW |
11 |
67,111,522 (GRCm39) |
nonsense |
probably null |
|
R2966:Myh1
|
UTSW |
11 |
67,105,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Myh1
|
UTSW |
11 |
67,096,423 (GRCm39) |
missense |
probably benign |
0.01 |
R4106:Myh1
|
UTSW |
11 |
67,102,403 (GRCm39) |
missense |
probably benign |
0.33 |
R4108:Myh1
|
UTSW |
11 |
67,102,403 (GRCm39) |
missense |
probably benign |
0.33 |
R4457:Myh1
|
UTSW |
11 |
67,111,441 (GRCm39) |
missense |
probably benign |
0.42 |
R4629:Myh1
|
UTSW |
11 |
67,100,119 (GRCm39) |
missense |
probably benign |
0.01 |
R4981:Myh1
|
UTSW |
11 |
67,115,300 (GRCm39) |
utr 3 prime |
probably benign |
|
R5032:Myh1
|
UTSW |
11 |
67,096,874 (GRCm39) |
nonsense |
probably null |
|
R5239:Myh1
|
UTSW |
11 |
67,106,051 (GRCm39) |
missense |
probably benign |
0.19 |
R5241:Myh1
|
UTSW |
11 |
67,095,275 (GRCm39) |
missense |
probably benign |
|
R5303:Myh1
|
UTSW |
11 |
67,092,843 (GRCm39) |
missense |
probably benign |
0.09 |
R5666:Myh1
|
UTSW |
11 |
67,112,178 (GRCm39) |
missense |
probably benign |
0.30 |
R5717:Myh1
|
UTSW |
11 |
67,099,782 (GRCm39) |
missense |
probably benign |
|
R5761:Myh1
|
UTSW |
11 |
67,110,078 (GRCm39) |
missense |
probably damaging |
0.98 |
R5870:Myh1
|
UTSW |
11 |
67,092,805 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6077:Myh1
|
UTSW |
11 |
67,102,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R6089:Myh1
|
UTSW |
11 |
67,111,613 (GRCm39) |
splice site |
probably null |
|
R6089:Myh1
|
UTSW |
11 |
67,092,993 (GRCm39) |
splice site |
probably null |
|
R6197:Myh1
|
UTSW |
11 |
67,111,793 (GRCm39) |
missense |
probably benign |
0.01 |
R6460:Myh1
|
UTSW |
11 |
67,112,202 (GRCm39) |
missense |
probably benign |
|
R6627:Myh1
|
UTSW |
11 |
67,105,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R6634:Myh1
|
UTSW |
11 |
67,099,890 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6725:Myh1
|
UTSW |
11 |
67,092,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Myh1
|
UTSW |
11 |
67,105,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R6813:Myh1
|
UTSW |
11 |
67,111,286 (GRCm39) |
missense |
probably benign |
0.34 |
R6866:Myh1
|
UTSW |
11 |
67,115,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R6997:Myh1
|
UTSW |
11 |
67,111,463 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7028:Myh1
|
UTSW |
11 |
67,111,247 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7133:Myh1
|
UTSW |
11 |
67,093,412 (GRCm39) |
missense |
probably benign |
|
R7185:Myh1
|
UTSW |
11 |
67,098,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R7283:Myh1
|
UTSW |
11 |
67,092,670 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7336:Myh1
|
UTSW |
11 |
67,111,435 (GRCm39) |
missense |
probably benign |
0.00 |
R7348:Myh1
|
UTSW |
11 |
67,093,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7369:Myh1
|
UTSW |
11 |
67,111,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Myh1
|
UTSW |
11 |
67,101,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7384:Myh1
|
UTSW |
11 |
67,115,201 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7387:Myh1
|
UTSW |
11 |
67,099,715 (GRCm39) |
missense |
probably benign |
0.14 |
R7424:Myh1
|
UTSW |
11 |
67,104,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Myh1
|
UTSW |
11 |
67,096,393 (GRCm39) |
nonsense |
probably null |
|
R7443:Myh1
|
UTSW |
11 |
67,111,331 (GRCm39) |
missense |
probably benign |
|
R7447:Myh1
|
UTSW |
11 |
67,110,006 (GRCm39) |
missense |
probably benign |
0.01 |
R7509:Myh1
|
UTSW |
11 |
67,101,287 (GRCm39) |
missense |
probably benign |
0.40 |
R7583:Myh1
|
UTSW |
11 |
67,111,739 (GRCm39) |
missense |
probably benign |
0.00 |
R7611:Myh1
|
UTSW |
11 |
67,101,243 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7617:Myh1
|
UTSW |
11 |
67,106,701 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7727:Myh1
|
UTSW |
11 |
67,106,748 (GRCm39) |
missense |
probably benign |
0.00 |
R8029:Myh1
|
UTSW |
11 |
67,102,066 (GRCm39) |
critical splice donor site |
probably null |
|
R8042:Myh1
|
UTSW |
11 |
67,097,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R8060:Myh1
|
UTSW |
11 |
67,106,077 (GRCm39) |
missense |
probably benign |
|
R8080:Myh1
|
UTSW |
11 |
67,102,228 (GRCm39) |
missense |
probably benign |
0.10 |
R8117:Myh1
|
UTSW |
11 |
67,113,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Myh1
|
UTSW |
11 |
67,093,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R8183:Myh1
|
UTSW |
11 |
67,092,832 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8397:Myh1
|
UTSW |
11 |
67,112,465 (GRCm39) |
missense |
probably damaging |
0.97 |
R8545:Myh1
|
UTSW |
11 |
67,093,027 (GRCm39) |
missense |
probably benign |
0.00 |
R8807:Myh1
|
UTSW |
11 |
67,111,354 (GRCm39) |
missense |
probably benign |
0.02 |
R8812:Myh1
|
UTSW |
11 |
67,099,967 (GRCm39) |
missense |
probably benign |
0.00 |
R8855:Myh1
|
UTSW |
11 |
67,102,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Myh1
|
UTSW |
11 |
67,096,739 (GRCm39) |
missense |
probably benign |
0.02 |
R8959:Myh1
|
UTSW |
11 |
67,102,328 (GRCm39) |
missense |
probably benign |
|
R8992:Myh1
|
UTSW |
11 |
67,096,607 (GRCm39) |
missense |
probably benign |
|
R9140:Myh1
|
UTSW |
11 |
67,100,089 (GRCm39) |
missense |
probably benign |
0.04 |
R9293:Myh1
|
UTSW |
11 |
67,099,929 (GRCm39) |
missense |
probably benign |
0.25 |
R9366:Myh1
|
UTSW |
11 |
67,110,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Myh1
|
UTSW |
11 |
67,110,631 (GRCm39) |
critical splice donor site |
probably null |
|
R9378:Myh1
|
UTSW |
11 |
67,093,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R9482:Myh1
|
UTSW |
11 |
67,108,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9507:Myh1
|
UTSW |
11 |
67,102,049 (GRCm39) |
missense |
probably benign |
0.00 |
R9558:Myh1
|
UTSW |
11 |
67,108,618 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9561:Myh1
|
UTSW |
11 |
67,108,618 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9587:Myh1
|
UTSW |
11 |
67,102,196 (GRCm39) |
missense |
probably benign |
0.03 |
X0062:Myh1
|
UTSW |
11 |
67,098,367 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Myh1
|
UTSW |
11 |
67,097,144 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Myh1
|
UTSW |
11 |
67,095,272 (GRCm39) |
missense |
probably benign |
|
Z1188:Myh1
|
UTSW |
11 |
67,095,272 (GRCm39) |
missense |
probably benign |
|
Z1190:Myh1
|
UTSW |
11 |
67,095,272 (GRCm39) |
missense |
probably benign |
|
Z1191:Myh1
|
UTSW |
11 |
67,095,272 (GRCm39) |
missense |
probably benign |
|
|