Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam5 |
T |
C |
8: 25,271,703 (GRCm39) |
D485G |
probably damaging |
Het |
Adamts19 |
T |
C |
18: 59,036,137 (GRCm39) |
|
probably null |
Het |
Adgrd1 |
A |
T |
5: 129,255,146 (GRCm39) |
I598F |
probably damaging |
Het |
Adh5 |
A |
G |
3: 138,157,174 (GRCm39) |
D245G |
probably benign |
Het |
Adra2b |
T |
C |
2: 127,206,212 (GRCm39) |
V238A |
probably benign |
Het |
Ank1 |
G |
A |
8: 23,606,258 (GRCm39) |
V1188I |
possibly damaging |
Het |
Asap1 |
C |
T |
15: 63,971,413 (GRCm39) |
G905D |
probably damaging |
Het |
AW554918 |
T |
C |
18: 25,477,959 (GRCm39) |
V428A |
probably benign |
Het |
Birc6 |
T |
A |
17: 74,950,436 (GRCm39) |
S3226T |
probably benign |
Het |
Cdh17 |
A |
T |
4: 11,785,280 (GRCm39) |
|
probably benign |
Het |
Cyfip2 |
A |
T |
11: 46,144,825 (GRCm39) |
Y676* |
probably null |
Het |
Dcaf17 |
T |
A |
2: 70,908,812 (GRCm39) |
|
probably benign |
Het |
Dclre1a |
A |
G |
19: 56,531,139 (GRCm39) |
F736L |
probably damaging |
Het |
Ddx41 |
A |
T |
13: 55,683,193 (GRCm39) |
H171Q |
possibly damaging |
Het |
Dennd5b |
G |
T |
6: 148,895,257 (GRCm39) |
Q1258K |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,584,295 (GRCm39) |
D137G |
probably damaging |
Het |
Dpyd |
G |
A |
3: 118,737,904 (GRCm39) |
V482I |
probably benign |
Het |
Erich6 |
A |
T |
3: 58,543,547 (GRCm39) |
|
probably benign |
Het |
Fam193b |
A |
G |
13: 55,702,024 (GRCm39) |
|
probably benign |
Het |
Foxp2 |
T |
C |
6: 15,405,643 (GRCm39) |
|
probably benign |
Het |
Frmd4a |
T |
C |
2: 4,577,252 (GRCm39) |
|
probably null |
Het |
Gas2l2 |
A |
G |
11: 83,313,693 (GRCm39) |
S540P |
possibly damaging |
Het |
Glis2 |
T |
C |
16: 4,431,517 (GRCm39) |
V348A |
probably benign |
Het |
Gm14443 |
C |
A |
2: 175,011,729 (GRCm39) |
G239V |
probably damaging |
Het |
Gpr158 |
T |
C |
2: 21,831,528 (GRCm39) |
V876A |
probably damaging |
Het |
H1f8 |
A |
G |
6: 115,926,942 (GRCm39) |
E273G |
probably benign |
Het |
Hadh |
C |
T |
3: 131,029,285 (GRCm39) |
D245N |
probably damaging |
Het |
Hk2 |
A |
T |
6: 82,711,957 (GRCm39) |
|
probably benign |
Het |
Ice1 |
A |
T |
13: 70,767,163 (GRCm39) |
Y108* |
probably null |
Het |
Il10ra |
T |
G |
9: 45,167,247 (GRCm39) |
M435L |
probably benign |
Het |
Inpp5k |
GT |
G |
11: 75,521,973 (GRCm39) |
|
probably null |
Het |
Kank4 |
G |
T |
4: 98,666,567 (GRCm39) |
P627T |
probably benign |
Het |
Kif16b |
A |
G |
2: 142,549,346 (GRCm39) |
|
probably benign |
Het |
Lipn |
A |
G |
19: 34,054,376 (GRCm39) |
I205V |
probably benign |
Het |
Miox |
C |
T |
15: 89,220,477 (GRCm39) |
L189F |
possibly damaging |
Het |
Myl3 |
A |
C |
9: 110,596,997 (GRCm39) |
D119A |
probably damaging |
Het |
Myo1d |
T |
G |
11: 80,448,349 (GRCm39) |
K925N |
probably benign |
Het |
Myoz1 |
T |
A |
14: 20,699,622 (GRCm39) |
M239L |
probably benign |
Het |
Ncoa6 |
TGC |
TGCGC |
2: 155,250,211 (GRCm39) |
|
probably null |
Het |
Nf1 |
C |
A |
11: 79,344,805 (GRCm39) |
|
probably benign |
Het |
Npepl1 |
C |
T |
2: 173,957,879 (GRCm39) |
P239S |
probably damaging |
Het |
Olfml1 |
A |
G |
7: 107,170,506 (GRCm39) |
K131R |
probably benign |
Het |
Or12k5 |
G |
A |
2: 36,895,462 (GRCm39) |
L55F |
probably damaging |
Het |
Or1e29 |
A |
G |
11: 73,667,935 (GRCm39) |
F73L |
possibly damaging |
Het |
Or1j15 |
T |
A |
2: 36,458,893 (GRCm39) |
Y94* |
probably null |
Het |
Or1j20 |
T |
C |
2: 36,760,022 (GRCm39) |
L148S |
possibly damaging |
Het |
Or4c10 |
T |
A |
2: 89,760,423 (GRCm39) |
I90K |
possibly damaging |
Het |
Or4f7 |
A |
C |
2: 111,644,213 (GRCm39) |
I286S |
probably damaging |
Het |
Or5p52 |
C |
T |
7: 107,502,212 (GRCm39) |
T96I |
probably benign |
Het |
Or6c202 |
C |
T |
10: 128,996,707 (GRCm39) |
D49N |
possibly damaging |
Het |
Pde7a |
T |
C |
3: 19,295,697 (GRCm39) |
|
probably benign |
Het |
Pik3c2g |
T |
C |
6: 139,903,519 (GRCm39) |
C591R |
probably benign |
Het |
Pkn2 |
T |
G |
3: 142,559,343 (GRCm39) |
K61Q |
probably damaging |
Het |
Ppfia1 |
C |
A |
7: 144,058,711 (GRCm39) |
G722C |
probably damaging |
Het |
Ppp1cb |
T |
C |
5: 32,644,958 (GRCm39) |
V263A |
probably damaging |
Het |
Rab11fip2 |
A |
T |
19: 59,895,567 (GRCm39) |
N440K |
possibly damaging |
Het |
Rbm34 |
T |
A |
8: 127,676,234 (GRCm39) |
K340N |
probably damaging |
Het |
Samd3 |
T |
C |
10: 26,147,399 (GRCm39) |
|
probably benign |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Sigirr |
T |
C |
7: 140,671,285 (GRCm39) |
D399G |
probably damaging |
Het |
Slc17a7 |
A |
G |
7: 44,824,371 (GRCm39) |
E554G |
probably benign |
Het |
Smc3 |
A |
G |
19: 53,589,993 (GRCm39) |
|
probably benign |
Het |
Tdrd1 |
T |
C |
19: 56,819,703 (GRCm39) |
Y68H |
probably benign |
Het |
Tespa1 |
T |
A |
10: 130,196,719 (GRCm39) |
L219Q |
probably damaging |
Het |
Tmem144 |
G |
A |
3: 79,746,580 (GRCm39) |
|
probably benign |
Het |
Ttc38 |
A |
G |
15: 85,740,673 (GRCm39) |
S436G |
probably benign |
Het |
Ttn |
T |
A |
2: 76,581,423 (GRCm39) |
I23157F |
probably damaging |
Het |
Ubxn2b |
T |
A |
4: 6,203,875 (GRCm39) |
|
probably benign |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Vmn2r72 |
T |
C |
7: 85,401,044 (GRCm39) |
E125G |
probably benign |
Het |
Vmn2r78 |
A |
T |
7: 86,572,235 (GRCm39) |
D532V |
probably benign |
Het |
Vwa8 |
C |
A |
14: 79,320,222 (GRCm39) |
L1078I |
probably benign |
Het |
Vwce |
A |
T |
19: 10,641,453 (GRCm39) |
|
probably null |
Het |
Zpr1 |
A |
G |
9: 46,190,995 (GRCm39) |
D300G |
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 |
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 |
67,112,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Myh1
|
UTSW |
11 |
67,096,751 (GRCm39) |
missense |
probably benign |
|
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 |
R7194:Myh1
|
UTSW |
11 |
67,102,183 (GRCm39) |
missense |
probably benign |
|
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 |
|
|