Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
G |
13: 77,471,735 (GRCm39) |
K1047E |
possibly damaging |
Het |
Aadacl2fm1 |
A |
G |
3: 59,839,110 (GRCm39) |
T11A |
possibly damaging |
Het |
Abca14 |
A |
T |
7: 119,807,191 (GRCm39) |
Y79F |
possibly damaging |
Het |
Abca2 |
T |
A |
2: 25,329,094 (GRCm39) |
M978K |
probably benign |
Het |
Adamts3 |
A |
T |
5: 89,848,269 (GRCm39) |
C684* |
probably null |
Het |
Adnp2 |
T |
C |
18: 80,172,637 (GRCm39) |
T591A |
probably benign |
Het |
Aff4 |
A |
T |
11: 53,263,306 (GRCm39) |
T109S |
probably damaging |
Het |
Agmo |
A |
G |
12: 37,293,720 (GRCm39) |
I48V |
probably benign |
Het |
Appl1 |
G |
A |
14: 26,649,784 (GRCm39) |
R581* |
probably null |
Het |
Armc9 |
A |
T |
1: 86,189,766 (GRCm39) |
M714L |
probably benign |
Het |
Atp6v0d2 |
T |
A |
4: 19,922,377 (GRCm39) |
T41S |
probably benign |
Het |
Bin1 |
A |
T |
18: 32,552,921 (GRCm39) |
Q182L |
probably damaging |
Het |
Bmp10 |
A |
G |
6: 87,410,684 (GRCm39) |
D159G |
probably benign |
Het |
Bsn |
G |
A |
9: 107,984,854 (GRCm39) |
P295S |
possibly damaging |
Het |
Cbx6 |
A |
G |
15: 79,712,606 (GRCm39) |
S274P |
probably damaging |
Het |
Cdc20b |
A |
G |
13: 113,192,631 (GRCm39) |
K108R |
probably benign |
Het |
Ces1d |
T |
A |
8: 93,912,724 (GRCm39) |
N238I |
probably damaging |
Het |
Col7a1 |
C |
T |
9: 108,787,708 (GRCm39) |
Q663* |
probably null |
Het |
Cpsf3 |
T |
C |
12: 21,358,039 (GRCm39) |
I517T |
possibly damaging |
Het |
Cyp2a5 |
C |
A |
7: 26,539,879 (GRCm39) |
T309N |
probably damaging |
Het |
Cyp2d40 |
A |
G |
15: 82,645,802 (GRCm39) |
F68L |
possibly damaging |
Het |
Cyp7b1 |
A |
T |
3: 18,150,837 (GRCm39) |
W301R |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,189,513 (GRCm39) |
N45I |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,621,776 (GRCm39) |
H1116Q |
probably benign |
Het |
Dntt |
A |
G |
19: 41,027,356 (GRCm39) |
N141S |
probably benign |
Het |
Fbxl13 |
T |
C |
5: 21,790,201 (GRCm39) |
N281D |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,559,410 (GRCm39) |
L1699H |
probably damaging |
Het |
Gabrr3 |
T |
C |
16: 59,282,037 (GRCm39) |
V464A |
possibly damaging |
Het |
Gdap1 |
T |
A |
1: 17,227,353 (GRCm39) |
I160N |
probably damaging |
Het |
Hnrnpll |
C |
A |
17: 80,369,291 (GRCm39) |
R44L |
unknown |
Het |
Hsp90ab1 |
T |
C |
17: 45,881,680 (GRCm39) |
E187G |
probably damaging |
Het |
Ighm |
T |
A |
12: 113,386,210 (GRCm39) |
T47S |
|
Het |
Itgb7 |
A |
C |
15: 102,135,831 (GRCm39) |
|
probably null |
Het |
Kif16b |
A |
T |
2: 142,461,738 (GRCm39) |
C1293* |
probably null |
Het |
Klf11 |
C |
T |
12: 24,705,043 (GRCm39) |
R166C |
probably benign |
Het |
Lca5l |
T |
A |
16: 95,977,212 (GRCm39) |
Q198L |
probably damaging |
Het |
Lnx2 |
A |
T |
5: 146,961,180 (GRCm39) |
M584K |
probably benign |
Het |
Lpp |
A |
T |
16: 24,540,737 (GRCm39) |
M1L |
probably benign |
Het |
Lrig3 |
A |
G |
10: 125,832,953 (GRCm39) |
T276A |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Megf8 |
A |
T |
7: 25,039,840 (GRCm39) |
|
probably null |
Het |
Neb |
C |
A |
2: 52,134,113 (GRCm39) |
R3290L |
possibly damaging |
Het |
Neb |
A |
C |
2: 52,137,304 (GRCm39) |
V220G |
|
Het |
Nktr |
A |
T |
9: 121,577,264 (GRCm39) |
K444I |
probably damaging |
Het |
Nol11 |
A |
T |
11: 107,064,505 (GRCm39) |
M483K |
probably benign |
Het |
Npy1r |
C |
A |
8: 67,156,861 (GRCm39) |
P94T |
probably damaging |
Het |
Nsmaf |
T |
C |
4: 6,440,940 (GRCm39) |
T37A |
probably benign |
Het |
Or10ad1b |
A |
G |
15: 98,124,920 (GRCm39) |
L204P |
possibly damaging |
Het |
Or2y3 |
G |
A |
17: 38,393,056 (GRCm39) |
A271V |
possibly damaging |
Het |
Or4c119 |
T |
C |
2: 88,987,399 (GRCm39) |
N40S |
probably damaging |
Het |
Or51v8 |
A |
T |
7: 103,319,389 (GRCm39) |
M283K |
probably damaging |
Het |
Or5w14 |
C |
A |
2: 87,541,423 (GRCm39) |
V276F |
possibly damaging |
Het |
Or8a1b |
A |
G |
9: 37,623,473 (GRCm39) |
I34T |
probably damaging |
Het |
Or8b37 |
G |
A |
9: 37,958,775 (GRCm39) |
V86M |
possibly damaging |
Het |
Palld |
C |
T |
8: 61,969,691 (GRCm39) |
R1211H |
unknown |
Het |
Pcdha3 |
A |
G |
18: 37,080,284 (GRCm39) |
D342G |
probably damaging |
Het |
Pclo |
G |
A |
5: 14,815,877 (GRCm39) |
V1266I |
|
Het |
Pcnx4 |
T |
C |
12: 72,602,664 (GRCm39) |
Y309H |
probably damaging |
Het |
Pde8a |
C |
T |
7: 80,982,619 (GRCm39) |
T746I |
probably damaging |
Het |
Pdzrn3 |
T |
G |
6: 101,127,772 (GRCm39) |
K965Q |
probably damaging |
Het |
Phldb1 |
G |
A |
9: 44,615,425 (GRCm39) |
A225V |
probably benign |
Het |
Pierce1 |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
2: 28,356,122 (GRCm39) |
|
probably benign |
Het |
Plat |
A |
G |
8: 23,265,599 (GRCm39) |
Y214C |
probably damaging |
Het |
Plppr1 |
T |
A |
4: 49,325,627 (GRCm39) |
C274* |
probably null |
Het |
Poglut1 |
A |
G |
16: 38,347,133 (GRCm39) |
F345L |
possibly damaging |
Het |
Ppara |
A |
T |
15: 85,661,837 (GRCm39) |
E26V |
possibly damaging |
Het |
Ppcdc |
A |
T |
9: 57,327,571 (GRCm39) |
W79R |
probably damaging |
Het |
Prdm1 |
C |
T |
10: 44,316,150 (GRCm39) |
C662Y |
probably damaging |
Het |
Sgms2 |
G |
A |
3: 131,136,011 (GRCm39) |
|
probably benign |
Het |
Slc31a1 |
T |
A |
4: 62,306,843 (GRCm39) |
M133K |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,777,998 (GRCm39) |
Q1309* |
probably null |
Het |
Sos1 |
T |
C |
17: 80,761,239 (GRCm39) |
I152M |
probably damaging |
Het |
Stk4 |
A |
T |
2: 163,952,136 (GRCm39) |
|
probably benign |
Het |
Syne1 |
T |
G |
10: 5,200,954 (GRCm39) |
N3538T |
probably damaging |
Het |
Tbc1d16 |
A |
G |
11: 119,099,666 (GRCm39) |
F236S |
probably damaging |
Het |
Tgs1 |
T |
A |
4: 3,595,475 (GRCm39) |
M548K |
probably benign |
Het |
Twf1 |
G |
A |
15: 94,483,336 (GRCm39) |
T124I |
probably damaging |
Het |
Tyro3 |
G |
A |
2: 119,642,648 (GRCm39) |
G611R |
probably damaging |
Het |
Unc13b |
T |
A |
4: 43,173,282 (GRCm39) |
I1370K |
unknown |
Het |
Usp40 |
A |
G |
1: 87,885,032 (GRCm39) |
W939R |
probably damaging |
Het |
Vamp8 |
A |
T |
6: 72,362,554 (GRCm39) |
V82E |
probably damaging |
Het |
Vmn2r17 |
A |
G |
5: 109,575,732 (GRCm39) |
H201R |
possibly damaging |
Het |
Whrn |
T |
C |
4: 63,350,079 (GRCm39) |
H546R |
probably benign |
Het |
Yeats2 |
T |
C |
16: 20,033,228 (GRCm39) |
V1036A |
probably benign |
Het |
Zfp352 |
T |
G |
4: 90,112,575 (GRCm39) |
N238K |
probably benign |
Het |
Zfp36l3 |
TCCAGGGGCGAGGGCAGCCCCAGGAGCAAGGGCCGCCCTAGGAATGAGGGCCGCCCCAGG |
TCCAGG |
X: 52,776,521 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,011,510 (GRCm39) |
S1159T |
probably benign |
Het |
Zscan4-ps1 |
A |
T |
7: 10,800,192 (GRCm39) |
H232Q |
probably benign |
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 |
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 |
|
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 |
|
|