Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,772,479 (GRCm39) |
K556R |
probably damaging |
Het |
4933406P04Rik |
A |
T |
10: 20,186,893 (GRCm39) |
|
probably benign |
Het |
Acmsd |
C |
A |
1: 127,687,493 (GRCm39) |
Y258* |
probably null |
Het |
Adgrf5 |
A |
T |
17: 43,761,973 (GRCm39) |
I1223F |
probably damaging |
Het |
Afp |
C |
T |
5: 90,638,655 (GRCm39) |
P6S |
probably benign |
Het |
Agap2 |
C |
A |
10: 126,927,540 (GRCm39) |
H1120Q |
probably damaging |
Het |
Angpt1 |
A |
G |
15: 42,375,800 (GRCm39) |
V152A |
probably damaging |
Het |
Ankrd1 |
A |
T |
19: 36,096,759 (GRCm39) |
F23I |
probably damaging |
Het |
Armc12 |
T |
C |
17: 28,757,869 (GRCm39) |
S334P |
possibly damaging |
Het |
Arnt2 |
C |
A |
7: 83,924,583 (GRCm39) |
D415Y |
probably damaging |
Het |
Cacna1s |
G |
T |
1: 136,004,592 (GRCm39) |
V131L |
probably benign |
Het |
Cacna2d2 |
T |
C |
9: 107,404,632 (GRCm39) |
V1141A |
possibly damaging |
Het |
Cfap61 |
T |
C |
2: 145,884,542 (GRCm39) |
L580P |
probably damaging |
Het |
Chga |
A |
T |
12: 102,522,164 (GRCm39) |
S23C |
probably damaging |
Het |
Chrna5 |
A |
G |
9: 54,912,159 (GRCm39) |
T320A |
probably damaging |
Het |
Col17a1 |
G |
T |
19: 47,639,301 (GRCm39) |
N1081K |
possibly damaging |
Het |
Cox7b2 |
A |
T |
5: 71,600,406 (GRCm39) |
C51S |
possibly damaging |
Het |
Cstdc3 |
T |
A |
16: 36,132,895 (GRCm39) |
D57E |
probably damaging |
Het |
Cwc22 |
A |
T |
2: 77,759,797 (GRCm39) |
D83E |
possibly damaging |
Het |
D130043K22Rik |
A |
C |
13: 25,067,877 (GRCm39) |
D871A |
probably damaging |
Het |
Dab2 |
A |
T |
15: 6,464,948 (GRCm39) |
M361L |
probably benign |
Het |
Dnah11 |
A |
C |
12: 117,880,523 (GRCm39) |
Y3866D |
probably damaging |
Het |
Dnmbp |
A |
G |
19: 43,890,159 (GRCm39) |
I536T |
probably benign |
Het |
Ehmt1 |
A |
T |
2: 24,774,302 (GRCm39) |
S43R |
probably damaging |
Het |
Ercc5 |
T |
C |
1: 44,212,540 (GRCm39) |
L666P |
probably benign |
Het |
F5 |
A |
G |
1: 164,010,403 (GRCm39) |
H378R |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,174,718 (GRCm39) |
N1998K |
probably damaging |
Het |
Fbxo28 |
T |
C |
1: 182,169,099 (GRCm39) |
D13G |
unknown |
Het |
Fras1 |
T |
C |
5: 96,857,741 (GRCm39) |
S2012P |
probably benign |
Het |
Gm5624 |
T |
A |
14: 44,799,302 (GRCm39) |
N41I |
probably damaging |
Het |
Gm8104 |
A |
G |
14: 42,959,028 (GRCm39) |
I73V |
possibly damaging |
Het |
Gpr141b |
T |
C |
13: 19,913,849 (GRCm39) |
|
noncoding transcript |
Het |
Gpr68 |
G |
A |
12: 100,845,167 (GRCm39) |
P126S |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,582,685 (GRCm39) |
T156S |
possibly damaging |
Het |
Hacl1 |
T |
A |
14: 31,336,221 (GRCm39) |
Y429F |
probably damaging |
Het |
Haus3 |
A |
C |
5: 34,320,916 (GRCm39) |
L510R |
probably damaging |
Het |
Helq |
C |
T |
5: 100,921,990 (GRCm39) |
G738D |
probably benign |
Het |
Hsd3b2 |
G |
C |
3: 98,619,553 (GRCm39) |
P131A |
probably damaging |
Het |
Il22ra1 |
G |
T |
4: 135,475,471 (GRCm39) |
C247F |
probably benign |
Het |
Ivl |
T |
C |
3: 92,479,891 (GRCm39) |
E58G |
unknown |
Het |
Kcnk9 |
G |
T |
15: 72,417,948 (GRCm39) |
Q61K |
probably benign |
Het |
Kremen1 |
CGGG |
CGGGGGG |
11: 5,151,791 (GRCm39) |
|
probably benign |
Het |
Loxhd1 |
G |
T |
18: 77,490,198 (GRCm39) |
A1314S |
probably damaging |
Het |
Lratd1 |
T |
C |
12: 14,200,226 (GRCm39) |
Y167C |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,259,175 (GRCm39) |
I1397V |
probably benign |
Het |
Lrig3 |
T |
A |
10: 125,832,920 (GRCm39) |
|
probably null |
Het |
Lrrc36 |
A |
G |
8: 106,176,397 (GRCm39) |
D378G |
probably damaging |
Het |
Lrrc49 |
G |
A |
9: 60,505,474 (GRCm39) |
T527I |
probably damaging |
Het |
Map4k4 |
C |
A |
1: 40,062,620 (GRCm39) |
T1195K |
probably damaging |
Het |
Mrps33 |
G |
A |
6: 39,779,429 (GRCm39) |
R89C |
probably damaging |
Het |
Mtor |
T |
C |
4: 148,547,349 (GRCm39) |
V444A |
probably benign |
Het |
Myo15b |
G |
T |
11: 115,771,335 (GRCm39) |
|
probably null |
Het |
Myo5c |
T |
C |
9: 75,153,446 (GRCm39) |
Y111H |
probably damaging |
Het |
Ncoa4-ps |
A |
T |
12: 119,225,506 (GRCm39) |
|
noncoding transcript |
Het |
Ndufv2 |
G |
C |
17: 66,390,481 (GRCm39) |
T163R |
probably damaging |
Het |
Nf1 |
A |
G |
11: 79,444,794 (GRCm39) |
N373S |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,962,917 (GRCm39) |
M834V |
probably benign |
Het |
Ogfod2 |
T |
C |
5: 124,253,019 (GRCm39) |
V343A |
probably damaging |
Het |
Or11g2 |
C |
T |
14: 50,856,143 (GRCm39) |
L155F |
probably benign |
Het |
Or11j4 |
C |
A |
14: 50,630,786 (GRCm39) |
S191* |
probably null |
Het |
Or3a1b |
A |
T |
11: 74,012,234 (GRCm39) |
T40S |
probably benign |
Het |
Or4c115 |
T |
A |
2: 88,928,050 (GRCm39) |
T74S |
probably benign |
Het |
Or51ag1 |
T |
C |
7: 103,155,248 (GRCm39) |
I302V |
possibly damaging |
Het |
Or52ab2 |
T |
A |
7: 102,969,621 (GRCm39) |
M1K |
probably null |
Het |
Or8g34 |
A |
T |
9: 39,373,410 (GRCm39) |
I228F |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,428,091 (GRCm39) |
|
probably null |
Het |
Ppp3ca |
A |
T |
3: 136,640,792 (GRCm39) |
I448F |
probably damaging |
Het |
Prss44 |
T |
C |
9: 110,646,272 (GRCm39) |
V333A |
probably damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Rars1 |
A |
C |
11: 35,716,822 (GRCm39) |
D231E |
probably benign |
Het |
Rfc1 |
T |
C |
5: 65,421,722 (GRCm39) |
Y1059C |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,652,719 (GRCm39) |
I2F |
probably damaging |
Het |
Sarm1 |
G |
T |
11: 78,381,820 (GRCm39) |
A221E |
possibly damaging |
Het |
Serpina3f |
A |
G |
12: 104,183,665 (GRCm39) |
T176A |
probably damaging |
Het |
Slc22a20 |
T |
C |
19: 6,035,695 (GRCm39) |
E131G |
probably benign |
Het |
Slc26a11 |
T |
C |
11: 119,263,979 (GRCm39) |
V343A |
probably damaging |
Het |
Slc2a4 |
A |
G |
11: 69,837,133 (GRCm39) |
I9T |
probably benign |
Het |
Slc39a6 |
G |
T |
18: 24,718,259 (GRCm39) |
D599E |
probably damaging |
Het |
Slc5a6 |
G |
T |
5: 31,198,020 (GRCm39) |
S285* |
probably null |
Het |
Spata9 |
A |
G |
13: 76,125,760 (GRCm39) |
H81R |
probably benign |
Het |
St7l |
A |
G |
3: 104,826,812 (GRCm39) |
E436G |
probably damaging |
Het |
Tecrl |
A |
G |
5: 83,427,077 (GRCm39) |
I357T |
probably damaging |
Het |
Thop1 |
C |
T |
10: 80,909,043 (GRCm39) |
R25C |
probably damaging |
Het |
Tmprss12 |
A |
G |
15: 100,190,428 (GRCm39) |
E266G |
probably benign |
Het |
Tpgs1 |
T |
A |
10: 79,511,344 (GRCm39) |
V162D |
possibly damaging |
Het |
Trpa1 |
C |
T |
1: 14,944,648 (GRCm39) |
R1032Q |
probably benign |
Het |
Tspan12 |
A |
G |
6: 21,795,699 (GRCm39) |
Y164H |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,135,274 (GRCm39) |
Y869H |
probably damaging |
Het |
Vmn1r21 |
A |
G |
6: 57,820,799 (GRCm39) |
I215T |
probably benign |
Het |
Zan |
A |
T |
5: 137,384,713 (GRCm39) |
S5104T |
unknown |
Het |
Zfp318 |
T |
C |
17: 46,722,980 (GRCm39) |
V1661A |
probably benign |
Het |
Zfp365 |
C |
T |
10: 67,724,772 (GRCm39) |
R372K |
probably damaging |
Het |
|
Other mutations in Myh2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Myh2
|
APN |
11 |
67,076,059 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00330:Myh2
|
APN |
11 |
67,084,266 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00423:Myh2
|
APN |
11 |
67,088,171 (GRCm39) |
missense |
probably benign |
|
IGL00429:Myh2
|
APN |
11 |
67,071,616 (GRCm39) |
nonsense |
probably null |
|
IGL00465:Myh2
|
APN |
11 |
67,069,659 (GRCm39) |
splice site |
probably benign |
|
IGL00671:Myh2
|
APN |
11 |
67,084,183 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00773:Myh2
|
APN |
11 |
67,085,247 (GRCm39) |
missense |
probably benign |
|
IGL00821:Myh2
|
APN |
11 |
67,088,223 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00900:Myh2
|
APN |
11 |
67,070,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Myh2
|
APN |
11 |
67,068,250 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01613:Myh2
|
APN |
11 |
67,088,170 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01845:Myh2
|
APN |
11 |
67,083,860 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01900:Myh2
|
APN |
11 |
67,074,609 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01936:Myh2
|
APN |
11 |
67,082,599 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02129:Myh2
|
APN |
11 |
67,076,084 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02172:Myh2
|
APN |
11 |
67,079,878 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02554:Myh2
|
APN |
11 |
67,079,991 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02578:Myh2
|
APN |
11 |
67,077,517 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03075:Myh2
|
APN |
11 |
67,071,662 (GRCm39) |
missense |
probably benign |
0.39 |
IGL03078:Myh2
|
APN |
11 |
67,081,256 (GRCm39) |
missense |
probably benign |
|
IGL03117:Myh2
|
APN |
11 |
67,071,710 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03255:Myh2
|
APN |
11 |
67,084,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03266:Myh2
|
APN |
11 |
67,067,150 (GRCm39) |
missense |
probably benign |
|
IGL03366:Myh2
|
APN |
11 |
67,074,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Myh2
|
APN |
11 |
67,080,395 (GRCm39) |
missense |
probably benign |
0.04 |
limp
|
UTSW |
11 |
67,083,330 (GRCm39) |
missense |
probably damaging |
1.00 |
noodle
|
UTSW |
11 |
67,077,438 (GRCm39) |
missense |
probably benign |
|
PIT4403001:Myh2
|
UTSW |
11 |
67,077,533 (GRCm39) |
missense |
probably benign |
0.22 |
PIT4508001:Myh2
|
UTSW |
11 |
67,076,331 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4677001:Myh2
|
UTSW |
11 |
67,072,818 (GRCm39) |
missense |
probably benign |
|
R0039:Myh2
|
UTSW |
11 |
67,069,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Myh2
|
UTSW |
11 |
67,076,130 (GRCm39) |
splice site |
probably benign |
|
R0389:Myh2
|
UTSW |
11 |
67,071,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R0400:Myh2
|
UTSW |
11 |
67,083,424 (GRCm39) |
splice site |
probably benign |
|
R0512:Myh2
|
UTSW |
11 |
67,079,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Myh2
|
UTSW |
11 |
67,069,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0746:Myh2
|
UTSW |
11 |
67,064,257 (GRCm39) |
missense |
probably benign |
0.00 |
R0842:Myh2
|
UTSW |
11 |
67,070,350 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0893:Myh2
|
UTSW |
11 |
67,077,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1218:Myh2
|
UTSW |
11 |
67,083,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R1264:Myh2
|
UTSW |
11 |
67,071,604 (GRCm39) |
missense |
probably damaging |
0.96 |
R1398:Myh2
|
UTSW |
11 |
67,076,113 (GRCm39) |
missense |
probably benign |
0.14 |
R1774:Myh2
|
UTSW |
11 |
67,064,300 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1829:Myh2
|
UTSW |
11 |
67,067,385 (GRCm39) |
missense |
probably damaging |
0.98 |
R1840:Myh2
|
UTSW |
11 |
67,077,313 (GRCm39) |
missense |
probably benign |
0.16 |
R1888:Myh2
|
UTSW |
11 |
67,071,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R1888:Myh2
|
UTSW |
11 |
67,071,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R1969:Myh2
|
UTSW |
11 |
67,080,004 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1971:Myh2
|
UTSW |
11 |
67,080,004 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1985:Myh2
|
UTSW |
11 |
67,071,740 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2021:Myh2
|
UTSW |
11 |
67,082,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Myh2
|
UTSW |
11 |
67,085,451 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2057:Myh2
|
UTSW |
11 |
67,079,665 (GRCm39) |
critical splice donor site |
probably null |
|
R2080:Myh2
|
UTSW |
11 |
67,065,767 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2142:Myh2
|
UTSW |
11 |
67,080,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2215:Myh2
|
UTSW |
11 |
67,082,563 (GRCm39) |
missense |
probably benign |
0.35 |
R2225:Myh2
|
UTSW |
11 |
67,084,555 (GRCm39) |
missense |
probably benign |
|
R2274:Myh2
|
UTSW |
11 |
67,081,184 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3018:Myh2
|
UTSW |
11 |
67,070,410 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3113:Myh2
|
UTSW |
11 |
67,076,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R3703:Myh2
|
UTSW |
11 |
67,080,427 (GRCm39) |
missense |
probably benign |
0.01 |
R4022:Myh2
|
UTSW |
11 |
67,070,230 (GRCm39) |
nonsense |
probably null |
|
R4081:Myh2
|
UTSW |
11 |
67,081,256 (GRCm39) |
missense |
probably benign |
0.11 |
R4191:Myh2
|
UTSW |
11 |
67,068,226 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4291:Myh2
|
UTSW |
11 |
67,071,985 (GRCm39) |
missense |
probably benign |
0.01 |
R4292:Myh2
|
UTSW |
11 |
67,085,723 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4424:Myh2
|
UTSW |
11 |
67,083,551 (GRCm39) |
missense |
probably benign |
0.01 |
R4524:Myh2
|
UTSW |
11 |
67,067,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Myh2
|
UTSW |
11 |
67,064,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4597:Myh2
|
UTSW |
11 |
67,080,244 (GRCm39) |
missense |
probably benign |
0.01 |
R4641:Myh2
|
UTSW |
11 |
67,085,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Myh2
|
UTSW |
11 |
67,079,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Myh2
|
UTSW |
11 |
67,079,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Myh2
|
UTSW |
11 |
67,077,328 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4818:Myh2
|
UTSW |
11 |
67,067,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Myh2
|
UTSW |
11 |
67,088,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4958:Myh2
|
UTSW |
11 |
67,083,785 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5139:Myh2
|
UTSW |
11 |
67,070,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Myh2
|
UTSW |
11 |
67,083,269 (GRCm39) |
missense |
probably benign |
0.00 |
R5306:Myh2
|
UTSW |
11 |
67,077,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R5492:Myh2
|
UTSW |
11 |
67,071,701 (GRCm39) |
missense |
probably benign |
0.20 |
R5503:Myh2
|
UTSW |
11 |
67,064,275 (GRCm39) |
missense |
probably benign |
|
R5646:Myh2
|
UTSW |
11 |
67,079,638 (GRCm39) |
missense |
probably benign |
0.07 |
R5750:Myh2
|
UTSW |
11 |
67,082,254 (GRCm39) |
missense |
probably benign |
|
R5806:Myh2
|
UTSW |
11 |
67,072,141 (GRCm39) |
missense |
probably damaging |
0.98 |
R5878:Myh2
|
UTSW |
11 |
67,083,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Myh2
|
UTSW |
11 |
67,076,002 (GRCm39) |
nonsense |
probably null |
|
R5898:Myh2
|
UTSW |
11 |
67,083,545 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6154:Myh2
|
UTSW |
11 |
67,077,438 (GRCm39) |
missense |
probably benign |
|
R6156:Myh2
|
UTSW |
11 |
67,071,879 (GRCm39) |
missense |
probably damaging |
0.98 |
R6236:Myh2
|
UTSW |
11 |
67,081,157 (GRCm39) |
missense |
probably benign |
0.00 |
R6349:Myh2
|
UTSW |
11 |
67,083,829 (GRCm39) |
missense |
probably benign |
0.04 |
R6441:Myh2
|
UTSW |
11 |
67,085,437 (GRCm39) |
missense |
probably benign |
0.00 |
R6548:Myh2
|
UTSW |
11 |
67,077,438 (GRCm39) |
missense |
probably benign |
|
R6681:Myh2
|
UTSW |
11 |
67,069,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Myh2
|
UTSW |
11 |
67,084,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R6925:Myh2
|
UTSW |
11 |
67,084,044 (GRCm39) |
missense |
probably benign |
0.00 |
R6969:Myh2
|
UTSW |
11 |
67,088,092 (GRCm39) |
missense |
probably benign |
|
R7172:Myh2
|
UTSW |
11 |
67,079,527 (GRCm39) |
missense |
probably benign |
0.00 |
R7257:Myh2
|
UTSW |
11 |
67,071,976 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7286:Myh2
|
UTSW |
11 |
67,079,195 (GRCm39) |
missense |
probably benign |
0.23 |
R7323:Myh2
|
UTSW |
11 |
67,088,191 (GRCm39) |
missense |
probably benign |
|
R7396:Myh2
|
UTSW |
11 |
67,085,554 (GRCm39) |
critical splice donor site |
probably null |
|
R7468:Myh2
|
UTSW |
11 |
67,083,368 (GRCm39) |
missense |
probably benign |
0.01 |
R7585:Myh2
|
UTSW |
11 |
67,070,237 (GRCm39) |
critical splice donor site |
probably null |
|
R7709:Myh2
|
UTSW |
11 |
67,085,690 (GRCm39) |
missense |
probably benign |
0.00 |
R7859:Myh2
|
UTSW |
11 |
67,077,526 (GRCm39) |
missense |
probably damaging |
0.96 |
R7908:Myh2
|
UTSW |
11 |
67,088,197 (GRCm39) |
missense |
probably benign |
|
R8062:Myh2
|
UTSW |
11 |
67,084,209 (GRCm39) |
nonsense |
probably null |
|
R8065:Myh2
|
UTSW |
11 |
67,072,170 (GRCm39) |
missense |
probably null |
0.01 |
R8093:Myh2
|
UTSW |
11 |
67,079,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Myh2
|
UTSW |
11 |
67,064,135 (GRCm39) |
missense |
probably benign |
|
R8235:Myh2
|
UTSW |
11 |
67,083,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8512:Myh2
|
UTSW |
11 |
67,081,187 (GRCm39) |
missense |
probably benign |
0.11 |
R8762:Myh2
|
UTSW |
11 |
67,084,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Myh2
|
UTSW |
11 |
67,083,398 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8777-TAIL:Myh2
|
UTSW |
11 |
67,083,398 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8823:Myh2
|
UTSW |
11 |
67,076,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R8927:Myh2
|
UTSW |
11 |
67,079,509 (GRCm39) |
missense |
probably benign |
0.00 |
R8928:Myh2
|
UTSW |
11 |
67,079,509 (GRCm39) |
missense |
probably benign |
0.00 |
R8978:Myh2
|
UTSW |
11 |
67,080,323 (GRCm39) |
missense |
probably damaging |
0.98 |
R8978:Myh2
|
UTSW |
11 |
67,068,188 (GRCm39) |
missense |
probably damaging |
0.96 |
R9228:Myh2
|
UTSW |
11 |
67,077,522 (GRCm39) |
missense |
probably benign |
0.11 |
R9332:Myh2
|
UTSW |
11 |
67,070,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R9404:Myh2
|
UTSW |
11 |
67,070,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R9430:Myh2
|
UTSW |
11 |
67,070,359 (GRCm39) |
missense |
probably benign |
0.01 |
R9445:Myh2
|
UTSW |
11 |
67,069,754 (GRCm39) |
missense |
probably damaging |
0.98 |
R9542:Myh2
|
UTSW |
11 |
67,072,002 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9597:Myh2
|
UTSW |
11 |
67,064,302 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9654:Myh2
|
UTSW |
11 |
67,088,171 (GRCm39) |
missense |
probably benign |
|
R9704:Myh2
|
UTSW |
11 |
67,071,617 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9736:Myh2
|
UTSW |
11 |
67,063,999 (GRCm39) |
missense |
probably benign |
0.00 |
R9740:Myh2
|
UTSW |
11 |
67,080,052 (GRCm39) |
missense |
probably damaging |
0.99 |
X0026:Myh2
|
UTSW |
11 |
67,065,848 (GRCm39) |
missense |
probably benign |
0.10 |
X0065:Myh2
|
UTSW |
11 |
67,067,085 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Myh2
|
UTSW |
11 |
67,071,589 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1088:Myh2
|
UTSW |
11 |
67,082,275 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Myh2
|
UTSW |
11 |
67,084,084 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Myh2
|
UTSW |
11 |
67,066,997 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1188:Myh2
|
UTSW |
11 |
67,079,639 (GRCm39) |
missense |
probably benign |
|
|