Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
G |
1: 156,450,104 (GRCm39) |
N90K |
possibly damaging |
Het |
Acox1 |
T |
C |
11: 116,069,001 (GRCm39) |
T415A |
possibly damaging |
Het |
Acy1 |
T |
C |
9: 106,314,921 (GRCm39) |
M1V |
probably null |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Alpk3 |
C |
A |
7: 80,750,746 (GRCm39) |
Y1505* |
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,390,902 (GRCm39) |
N2256S |
probably benign |
Het |
Ankrd22 |
C |
A |
19: 34,126,692 (GRCm39) |
C46F |
possibly damaging |
Het |
Arhgef5 |
A |
T |
6: 43,257,605 (GRCm39) |
K1291* |
probably null |
Het |
Arl9 |
T |
A |
5: 77,158,276 (GRCm39) |
Y119* |
probably null |
Het |
Asb14 |
T |
C |
14: 26,622,805 (GRCm39) |
V89A |
probably benign |
Het |
Banp |
T |
G |
8: 122,676,588 (GRCm39) |
|
probably null |
Het |
Btn2a2 |
T |
C |
13: 23,666,933 (GRCm39) |
N224S |
probably benign |
Het |
C1ra |
C |
T |
6: 124,499,403 (GRCm39) |
Q530* |
probably null |
Het |
C2cd6 |
A |
C |
1: 59,107,844 (GRCm39) |
S273A |
probably benign |
Het |
Cd1d2 |
A |
T |
3: 86,895,583 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
T |
C |
12: 111,306,307 (GRCm39) |
D132G |
probably damaging |
Het |
Cfap45 |
C |
A |
1: 172,362,877 (GRCm39) |
Y289* |
probably null |
Het |
Chrdl2 |
T |
C |
7: 99,659,332 (GRCm39) |
|
probably null |
Het |
Cilk1 |
A |
G |
9: 78,065,221 (GRCm39) |
K377R |
probably benign |
Het |
Cst5 |
C |
T |
2: 149,247,496 (GRCm39) |
L71F |
probably benign |
Het |
Dcaf11 |
T |
C |
14: 55,802,966 (GRCm39) |
F292L |
possibly damaging |
Het |
Dgcr8 |
A |
G |
16: 18,077,487 (GRCm39) |
F641S |
probably damaging |
Het |
Dnm3 |
G |
A |
1: 162,149,198 (GRCm39) |
|
probably null |
Het |
Efcab3 |
G |
T |
11: 104,640,526 (GRCm39) |
S1088I |
probably benign |
Het |
Eral1 |
T |
C |
11: 77,966,219 (GRCm39) |
K320E |
probably damaging |
Het |
Eva1a |
A |
G |
6: 82,069,002 (GRCm39) |
T110A |
possibly damaging |
Het |
Fbxo42 |
A |
G |
4: 140,926,917 (GRCm39) |
D399G |
possibly damaging |
Het |
Frs2 |
T |
C |
10: 116,910,007 (GRCm39) |
T452A |
possibly damaging |
Het |
Git2 |
T |
A |
5: 114,871,958 (GRCm39) |
D542V |
probably damaging |
Het |
Grk2 |
T |
A |
19: 4,356,063 (GRCm39) |
|
probably benign |
Het |
Gsg1l2 |
A |
G |
11: 67,676,110 (GRCm39) |
N158S |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,918,063 (GRCm39) |
N740S |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,791,588 (GRCm39) |
|
probably null |
Het |
Hemk1 |
A |
G |
9: 107,208,288 (GRCm39) |
|
probably null |
Het |
Hormad2 |
G |
T |
11: 4,362,245 (GRCm39) |
Y126* |
probably null |
Het |
Hr |
A |
G |
14: 70,795,652 (GRCm39) |
E399G |
possibly damaging |
Het |
Ilf3 |
C |
A |
9: 21,314,707 (GRCm39) |
H780N |
unknown |
Het |
Inpp5e |
A |
T |
2: 26,298,161 (GRCm39) |
S147T |
probably benign |
Het |
Irag2 |
C |
A |
6: 145,119,427 (GRCm39) |
|
probably null |
Het |
Jmjd6 |
T |
C |
11: 116,733,275 (GRCm39) |
D134G |
probably damaging |
Het |
Kif23 |
G |
T |
9: 61,844,457 (GRCm39) |
Y120* |
probably null |
Het |
Klk12 |
T |
A |
7: 43,422,780 (GRCm39) |
Y236N |
probably damaging |
Het |
Kmt5b |
C |
A |
19: 3,852,799 (GRCm39) |
Y186* |
probably null |
Het |
Krtap9-5 |
A |
G |
11: 99,840,132 (GRCm39) |
T278A |
unknown |
Het |
Lca5 |
T |
A |
9: 83,305,509 (GRCm39) |
D99V |
probably damaging |
Het |
Leng9 |
A |
G |
7: 4,151,800 (GRCm39) |
V292A |
probably benign |
Het |
Lime1 |
A |
G |
2: 181,025,135 (GRCm39) |
R231G |
probably benign |
Het |
Mctp2 |
T |
A |
7: 71,861,438 (GRCm39) |
E402D |
probably damaging |
Het |
Mrpl28 |
T |
A |
17: 26,343,589 (GRCm39) |
S116R |
probably damaging |
Het |
Muc15 |
A |
T |
2: 110,561,862 (GRCm39) |
R99S |
probably benign |
Het |
Mynn |
T |
A |
3: 30,657,825 (GRCm39) |
Y48N |
probably damaging |
Het |
Myo1b |
A |
T |
1: 51,836,639 (GRCm39) |
V274E |
possibly damaging |
Het |
Nemp1 |
T |
A |
10: 127,528,923 (GRCm39) |
M209K |
possibly damaging |
Het |
Nlrc4 |
G |
T |
17: 74,752,507 (GRCm39) |
D625E |
probably benign |
Het |
Or10al6 |
C |
T |
17: 38,082,910 (GRCm39) |
A122V |
probably damaging |
Het |
Or11a4 |
T |
C |
17: 37,536,276 (GRCm39) |
F87L |
probably benign |
Het |
Or4p4 |
T |
C |
2: 88,482,622 (GRCm39) |
L42P |
probably damaging |
Het |
Otog |
T |
C |
7: 45,913,543 (GRCm39) |
V792A |
probably benign |
Het |
Paqr8 |
T |
C |
1: 21,005,442 (GRCm39) |
Y199H |
probably damaging |
Het |
Popdc3 |
A |
G |
10: 45,191,117 (GRCm39) |
D76G |
probably damaging |
Het |
Ppme1 |
T |
C |
7: 99,991,069 (GRCm39) |
N210D |
probably benign |
Het |
Prdm15 |
A |
C |
16: 97,636,842 (GRCm39) |
Y158* |
probably null |
Het |
Prrg2 |
A |
T |
7: 44,709,687 (GRCm39) |
L70Q |
probably benign |
Het |
Psmg4 |
C |
T |
13: 34,361,966 (GRCm39) |
R85W |
probably damaging |
Het |
Rab11fip4 |
A |
T |
11: 79,580,478 (GRCm39) |
T437S |
probably benign |
Het |
Rap2a |
T |
A |
14: 120,716,338 (GRCm39) |
M67K |
probably damaging |
Het |
Rnf123 |
A |
T |
9: 107,946,208 (GRCm39) |
H322Q |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,990,801 (GRCm39) |
T521S |
possibly damaging |
Het |
Scrn2 |
T |
G |
11: 96,923,992 (GRCm39) |
V292G |
possibly damaging |
Het |
Serpina3n |
C |
A |
12: 104,377,656 (GRCm39) |
P303H |
probably benign |
Het |
Spop |
C |
T |
11: 95,376,727 (GRCm39) |
T260M |
probably damaging |
Het |
Surf2 |
G |
A |
2: 26,809,354 (GRCm39) |
G224D |
probably benign |
Het |
Synm |
T |
G |
7: 67,382,971 (GRCm39) |
N669T |
unknown |
Het |
Tmprss13 |
T |
C |
9: 45,239,721 (GRCm39) |
S10P |
unknown |
Het |
Trav9d-1 |
T |
A |
14: 53,029,970 (GRCm39) |
S25T |
probably benign |
Het |
Trpc3 |
A |
T |
3: 36,678,565 (GRCm39) |
I840K |
probably damaging |
Het |
Tsbp1 |
T |
A |
17: 34,636,539 (GRCm39) |
|
probably null |
Het |
Tssc4 |
C |
A |
7: 142,622,999 (GRCm39) |
|
probably benign |
Het |
Ttc39d |
G |
T |
17: 80,523,579 (GRCm39) |
R79S |
possibly damaging |
Het |
Txlnb |
T |
A |
10: 17,675,082 (GRCm39) |
S78R |
probably damaging |
Het |
Vmn1r142 |
T |
A |
7: 21,862,784 (GRCm39) |
Q226L |
possibly damaging |
Het |
Vmn1r230 |
T |
C |
17: 21,067,146 (GRCm39) |
S112P |
probably damaging |
Het |
Wrnip1 |
T |
C |
13: 33,000,360 (GRCm39) |
F456L |
possibly damaging |
Het |
Zc3h8 |
G |
T |
2: 128,775,215 (GRCm39) |
H148Q |
probably benign |
Het |
Zcchc3 |
A |
G |
2: 152,256,615 (GRCm39) |
V28A |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,346,669 (GRCm39) |
C1683S |
probably benign |
Het |
Zfp874a |
T |
C |
13: 67,573,723 (GRCm39) |
|
probably null |
Het |
Zmym4 |
A |
G |
4: 126,776,029 (GRCm39) |
S1260P |
probably benign |
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 |
R1800:Myh2
|
UTSW |
11 |
67,079,764 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|
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 |
|
|