Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
A |
T |
16: 97,867,367 (GRCm39) |
H198Q |
probably damaging |
Het |
Abcb9 |
T |
C |
5: 124,221,706 (GRCm39) |
T223A |
probably benign |
Het |
Actc1 |
T |
A |
2: 113,880,881 (GRCm39) |
K115* |
probably null |
Het |
Angptl2 |
G |
A |
2: 33,132,316 (GRCm39) |
D308N |
probably benign |
Het |
Arl4d |
A |
C |
11: 101,557,892 (GRCm39) |
Q139H |
possibly damaging |
Het |
Aspm |
T |
A |
1: 139,418,125 (GRCm39) |
C2951* |
probably null |
Het |
Atp23 |
A |
T |
10: 126,723,362 (GRCm39) |
*247R |
probably null |
Het |
B3gnt7 |
T |
A |
1: 86,232,839 (GRCm39) |
S28R |
probably benign |
Het |
Bmp7 |
C |
T |
2: 172,721,211 (GRCm39) |
R288H |
probably damaging |
Het |
Bsdc1 |
G |
T |
4: 129,355,439 (GRCm39) |
|
probably benign |
Het |
Capn13 |
T |
C |
17: 73,631,761 (GRCm39) |
|
probably null |
Het |
Ccdc146 |
T |
C |
5: 21,538,060 (GRCm39) |
E88G |
probably damaging |
Het |
Ccdc73 |
C |
A |
2: 104,822,542 (GRCm39) |
D2E |
|
Het |
Cdc5l |
C |
A |
17: 45,721,839 (GRCm39) |
R477L |
|
Het |
Cdh22 |
T |
A |
2: 164,965,504 (GRCm39) |
H529L |
possibly damaging |
Het |
Chchd3 |
T |
A |
6: 32,780,951 (GRCm39) |
E178D |
probably benign |
Het |
Ciz1 |
A |
T |
2: 32,257,512 (GRCm39) |
R186* |
probably null |
Het |
Col4a2 |
A |
G |
8: 11,475,543 (GRCm39) |
|
probably null |
Het |
Copa |
T |
A |
1: 171,931,737 (GRCm39) |
H329Q |
probably null |
Het |
Dcaf7 |
A |
G |
11: 105,942,752 (GRCm39) |
D233G |
probably damaging |
Het |
Dclk2 |
G |
T |
3: 86,739,048 (GRCm39) |
P317Q |
probably damaging |
Het |
Dgat2 |
T |
C |
7: 98,818,710 (GRCm39) |
Y90C |
probably benign |
Het |
Dsc3 |
A |
T |
18: 20,107,234 (GRCm39) |
H462Q |
probably benign |
Het |
Fam151a |
T |
A |
4: 106,603,242 (GRCm39) |
|
probably benign |
Het |
Fn1 |
T |
C |
1: 71,638,535 (GRCm39) |
N1998S |
probably benign |
Het |
Fpr2 |
T |
C |
17: 18,113,724 (GRCm39) |
L240S |
possibly damaging |
Het |
Fzd9 |
A |
T |
5: 135,278,589 (GRCm39) |
M432K |
probably damaging |
Het |
Gm5862 |
T |
A |
5: 26,226,678 (GRCm39) |
I75F |
probably damaging |
Het |
Gpr45 |
T |
A |
1: 43,072,314 (GRCm39) |
V319D |
probably damaging |
Het |
H4c11 |
T |
C |
13: 21,919,525 (GRCm39) |
V87A |
possibly damaging |
Het |
Igfn1 |
T |
A |
1: 135,905,984 (GRCm39) |
R275W |
probably damaging |
Het |
Inafm1 |
G |
A |
7: 16,006,980 (GRCm39) |
A79V |
unknown |
Het |
Itfg1 |
C |
T |
8: 86,567,420 (GRCm39) |
|
probably benign |
Het |
Kcnt2 |
T |
A |
1: 140,356,535 (GRCm39) |
|
probably null |
Het |
Klhl35 |
T |
G |
7: 99,120,221 (GRCm39) |
I366S |
probably damaging |
Het |
Lysmd1 |
A |
T |
3: 95,045,831 (GRCm39) |
I223F |
probably damaging |
Het |
Mrps30 |
A |
G |
13: 118,523,205 (GRCm39) |
L189P |
probably damaging |
Het |
Ms4a4d |
A |
C |
19: 11,533,574 (GRCm39) |
T152P |
probably benign |
Het |
Mtcl1 |
A |
T |
17: 66,755,628 (GRCm39) |
I238K |
probably benign |
Het |
Musk |
T |
C |
4: 58,301,638 (GRCm39) |
I132T |
probably damaging |
Het |
Myh2 |
A |
T |
11: 67,079,509 (GRCm39) |
M989L |
probably benign |
Het |
Nt5c1a |
C |
T |
4: 123,102,281 (GRCm39) |
T69M |
possibly damaging |
Het |
Nuak2 |
T |
A |
1: 132,255,916 (GRCm39) |
D196E |
probably damaging |
Het |
Or52h7 |
A |
T |
7: 104,214,229 (GRCm39) |
H267L |
probably damaging |
Het |
Or5ap2 |
A |
T |
2: 85,679,918 (GRCm39) |
I41F |
possibly damaging |
Het |
Or5t7 |
T |
C |
2: 86,507,630 (GRCm39) |
T16A |
probably benign |
Het |
Or8k53 |
T |
C |
2: 86,178,090 (GRCm39) |
T7A |
possibly damaging |
Het |
Or8s10 |
A |
G |
15: 98,336,519 (GRCm39) |
|
probably benign |
Het |
Palb2 |
A |
T |
7: 121,723,821 (GRCm39) |
C643S |
probably damaging |
Het |
Pde5a |
T |
A |
3: 122,633,249 (GRCm39) |
I706N |
probably damaging |
Het |
Pdlim4 |
T |
C |
11: 53,950,790 (GRCm39) |
R100G |
probably benign |
Het |
Pip5k1c |
T |
A |
10: 81,128,906 (GRCm39) |
V5E |
possibly damaging |
Het |
Pira1 |
A |
C |
7: 3,742,358 (GRCm39) |
N56K |
probably benign |
Het |
Plekhm1 |
A |
G |
11: 103,268,039 (GRCm39) |
V644A |
probably benign |
Het |
Plk2 |
T |
G |
13: 110,535,750 (GRCm39) |
V524G |
probably damaging |
Het |
Ppl |
T |
A |
16: 4,905,474 (GRCm39) |
N1607I |
probably benign |
Het |
Prag1 |
T |
G |
8: 36,614,360 (GRCm39) |
V1304G |
probably damaging |
Het |
Prex1 |
C |
T |
2: 166,426,995 (GRCm39) |
V1077M |
probably damaging |
Het |
Prmt6 |
T |
C |
3: 110,158,248 (GRCm39) |
S14G |
probably benign |
Het |
Psrc1 |
T |
G |
3: 108,293,973 (GRCm39) |
S263R |
probably damaging |
Het |
Qrfprl |
C |
A |
6: 65,358,597 (GRCm39) |
S107* |
probably null |
Het |
Rbp7 |
A |
T |
4: 149,537,958 (GRCm39) |
L36* |
probably null |
Het |
Rgs12 |
G |
T |
5: 35,123,633 (GRCm39) |
W472L |
possibly damaging |
Het |
Rrp8 |
C |
A |
7: 105,384,073 (GRCm39) |
C143F |
possibly damaging |
Het |
Sart1 |
T |
C |
19: 5,438,529 (GRCm39) |
S43G |
probably benign |
Het |
Setx |
A |
G |
2: 29,016,971 (GRCm39) |
T25A |
possibly damaging |
Het |
Skint5 |
G |
A |
4: 113,341,099 (GRCm39) |
T1414I |
probably benign |
Het |
Sorbs2 |
T |
A |
8: 46,248,952 (GRCm39) |
S734R |
probably damaging |
Het |
Spata31g1 |
A |
T |
4: 42,972,251 (GRCm39) |
Y528F |
probably benign |
Het |
Spon1 |
T |
C |
7: 113,629,592 (GRCm39) |
|
probably null |
Het |
Sptbn1 |
C |
T |
11: 30,088,962 (GRCm39) |
V767I |
probably damaging |
Het |
Srf |
T |
C |
17: 46,860,095 (GRCm39) |
I477V |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,701,331 (GRCm39) |
Y282C |
probably damaging |
Het |
Tbc1d23 |
A |
G |
16: 56,992,152 (GRCm39) |
Y603H |
probably damaging |
Het |
Tdpoz6 |
T |
A |
3: 93,599,950 (GRCm39) |
T140S |
probably benign |
Het |
Tfap4 |
T |
C |
16: 4,369,218 (GRCm39) |
D134G |
probably damaging |
Het |
Tmem200c |
A |
G |
17: 69,148,733 (GRCm39) |
T439A |
probably benign |
Het |
Tmem63b |
A |
T |
17: 45,975,908 (GRCm39) |
M515K |
probably damaging |
Het |
Tnc |
A |
T |
4: 63,925,595 (GRCm39) |
N980K |
probably damaging |
Het |
Ttc23l |
T |
A |
15: 10,530,720 (GRCm39) |
L297F |
probably damaging |
Het |
Vinac1 |
A |
G |
2: 128,882,789 (GRCm39) |
S76P |
|
Het |
Vmn1r170 |
A |
G |
7: 23,305,814 (GRCm39) |
N72S |
possibly damaging |
Het |
Vmn2r8 |
T |
C |
5: 108,950,131 (GRCm39) |
M239V |
|
Het |
Vopp1 |
A |
G |
6: 57,731,578 (GRCm39) |
F138L |
probably damaging |
Het |
Vps41 |
T |
A |
13: 18,929,501 (GRCm39) |
F79I |
probably benign |
Het |
Zfp317 |
T |
C |
9: 19,552,521 (GRCm39) |
M1T |
probably null |
Het |
|
Other mutations in Myh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Myh8
|
APN |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01020:Myh8
|
APN |
11 |
67,174,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01348:Myh8
|
APN |
11 |
67,188,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01382:Myh8
|
APN |
11 |
67,192,799 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01454:Myh8
|
APN |
11 |
67,174,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Myh8
|
APN |
11 |
67,183,505 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01472:Myh8
|
APN |
11 |
67,179,205 (GRCm39) |
splice site |
probably benign |
|
IGL01473:Myh8
|
APN |
11 |
67,192,651 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01613:Myh8
|
APN |
11 |
67,192,536 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01763:Myh8
|
APN |
11 |
67,177,245 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01828:Myh8
|
APN |
11 |
67,194,652 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01862:Myh8
|
APN |
11 |
67,180,520 (GRCm39) |
nonsense |
probably null |
|
IGL01905:Myh8
|
APN |
11 |
67,175,477 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02280:Myh8
|
APN |
11 |
67,174,198 (GRCm39) |
unclassified |
probably benign |
|
IGL02386:Myh8
|
APN |
11 |
67,185,266 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02449:Myh8
|
APN |
11 |
67,185,440 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02500:Myh8
|
APN |
11 |
67,196,536 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02745:Myh8
|
APN |
11 |
67,188,327 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02799:Myh8
|
APN |
11 |
67,192,418 (GRCm39) |
splice site |
probably benign |
|
IGL03063:Myh8
|
APN |
11 |
67,179,031 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03223:Myh8
|
APN |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03336:Myh8
|
APN |
11 |
67,175,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03338:Myh8
|
APN |
11 |
67,189,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Myh8
|
APN |
11 |
67,194,739 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03392:Myh8
|
APN |
11 |
67,185,244 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB009:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
BB013:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB019:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Myh8
|
UTSW |
11 |
67,180,456 (GRCm39) |
missense |
probably benign |
0.01 |
R0012:Myh8
|
UTSW |
11 |
67,190,847 (GRCm39) |
missense |
probably benign |
0.02 |
R0016:Myh8
|
UTSW |
11 |
67,189,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Myh8
|
UTSW |
11 |
67,189,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Myh8
|
UTSW |
11 |
67,197,090 (GRCm39) |
splice site |
probably benign |
|
R0131:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0131:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0132:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0238:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0393:Myh8
|
UTSW |
11 |
67,196,843 (GRCm39) |
splice site |
probably benign |
|
R0453:Myh8
|
UTSW |
11 |
67,183,731 (GRCm39) |
missense |
probably benign |
0.03 |
R0454:Myh8
|
UTSW |
11 |
67,194,591 (GRCm39) |
nonsense |
probably null |
|
R0466:Myh8
|
UTSW |
11 |
67,189,405 (GRCm39) |
missense |
probably benign |
0.01 |
R0487:Myh8
|
UTSW |
11 |
67,192,837 (GRCm39) |
missense |
probably benign |
|
R0511:Myh8
|
UTSW |
11 |
67,175,333 (GRCm39) |
missense |
probably benign |
0.01 |
R0557:Myh8
|
UTSW |
11 |
67,192,624 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0589:Myh8
|
UTSW |
11 |
67,189,453 (GRCm39) |
missense |
probably benign |
0.00 |
R0658:Myh8
|
UTSW |
11 |
67,175,358 (GRCm39) |
critical splice donor site |
probably null |
|
R0782:Myh8
|
UTSW |
11 |
67,180,580 (GRCm39) |
missense |
probably benign |
0.16 |
R0829:Myh8
|
UTSW |
11 |
67,174,326 (GRCm39) |
unclassified |
probably benign |
|
R0845:Myh8
|
UTSW |
11 |
67,177,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Myh8
|
UTSW |
11 |
67,196,824 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0972:Myh8
|
UTSW |
11 |
67,188,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Myh8
|
UTSW |
11 |
67,187,957 (GRCm39) |
nonsense |
probably null |
|
R1417:Myh8
|
UTSW |
11 |
67,197,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Myh8
|
UTSW |
11 |
67,183,551 (GRCm39) |
missense |
probably benign |
0.23 |
R1497:Myh8
|
UTSW |
11 |
67,180,638 (GRCm39) |
missense |
probably benign |
0.00 |
R1605:Myh8
|
UTSW |
11 |
67,192,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R1701:Myh8
|
UTSW |
11 |
67,170,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Myh8
|
UTSW |
11 |
67,169,830 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1989:Myh8
|
UTSW |
11 |
67,183,550 (GRCm39) |
missense |
probably benign |
0.00 |
R2010:Myh8
|
UTSW |
11 |
67,187,990 (GRCm39) |
nonsense |
probably null |
|
R2095:Myh8
|
UTSW |
11 |
67,177,050 (GRCm39) |
missense |
probably benign |
0.00 |
R2132:Myh8
|
UTSW |
11 |
67,183,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Myh8
|
UTSW |
11 |
67,185,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R2229:Myh8
|
UTSW |
11 |
67,199,174 (GRCm39) |
missense |
probably damaging |
0.98 |
R2302:Myh8
|
UTSW |
11 |
67,177,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Myh8
|
UTSW |
11 |
67,185,344 (GRCm39) |
missense |
probably benign |
0.03 |
R2429:Myh8
|
UTSW |
11 |
67,194,723 (GRCm39) |
missense |
probably benign |
0.21 |
R2880:Myh8
|
UTSW |
11 |
67,188,090 (GRCm39) |
missense |
probably damaging |
0.97 |
R3692:Myh8
|
UTSW |
11 |
67,192,744 (GRCm39) |
missense |
probably damaging |
0.98 |
R3756:Myh8
|
UTSW |
11 |
67,175,443 (GRCm39) |
unclassified |
probably benign |
|
R3924:Myh8
|
UTSW |
11 |
67,187,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R4172:Myh8
|
UTSW |
11 |
67,183,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R4255:Myh8
|
UTSW |
11 |
67,190,560 (GRCm39) |
missense |
probably benign |
|
R4621:Myh8
|
UTSW |
11 |
67,177,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Myh8
|
UTSW |
11 |
67,177,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Myh8
|
UTSW |
11 |
67,170,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Myh8
|
UTSW |
11 |
67,183,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Myh8
|
UTSW |
11 |
67,196,742 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5119:Myh8
|
UTSW |
11 |
67,189,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Myh8
|
UTSW |
11 |
67,179,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R5229:Myh8
|
UTSW |
11 |
67,175,310 (GRCm39) |
missense |
probably damaging |
0.96 |
R5320:Myh8
|
UTSW |
11 |
67,177,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Myh8
|
UTSW |
11 |
67,192,244 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5523:Myh8
|
UTSW |
11 |
67,196,788 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5540:Myh8
|
UTSW |
11 |
67,177,266 (GRCm39) |
missense |
probably benign |
0.00 |
R5726:Myh8
|
UTSW |
11 |
67,185,392 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5770:Myh8
|
UTSW |
11 |
67,188,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Myh8
|
UTSW |
11 |
67,188,326 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6253:Myh8
|
UTSW |
11 |
67,192,793 (GRCm39) |
missense |
probably benign |
0.06 |
R6318:Myh8
|
UTSW |
11 |
67,190,167 (GRCm39) |
missense |
probably benign |
0.00 |
R6432:Myh8
|
UTSW |
11 |
67,189,405 (GRCm39) |
missense |
probably benign |
0.01 |
R6452:Myh8
|
UTSW |
11 |
67,196,565 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6452:Myh8
|
UTSW |
11 |
67,183,275 (GRCm39) |
missense |
probably benign |
0.27 |
R6512:Myh8
|
UTSW |
11 |
67,180,488 (GRCm39) |
nonsense |
probably null |
|
R6714:Myh8
|
UTSW |
11 |
67,197,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Myh8
|
UTSW |
11 |
67,175,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Myh8
|
UTSW |
11 |
67,179,142 (GRCm39) |
missense |
probably benign |
0.03 |
R7025:Myh8
|
UTSW |
11 |
67,188,365 (GRCm39) |
missense |
probably benign |
0.02 |
R7086:Myh8
|
UTSW |
11 |
67,183,453 (GRCm39) |
splice site |
probably null |
|
R7098:Myh8
|
UTSW |
11 |
67,169,879 (GRCm39) |
missense |
probably benign |
0.03 |
R7498:Myh8
|
UTSW |
11 |
67,174,263 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7716:Myh8
|
UTSW |
11 |
67,189,478 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7765:Myh8
|
UTSW |
11 |
67,194,481 (GRCm39) |
missense |
probably benign |
0.44 |
R7825:Myh8
|
UTSW |
11 |
67,194,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7921:Myh8
|
UTSW |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
R7926:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7932:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
R8003:Myh8
|
UTSW |
11 |
67,190,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Myh8
|
UTSW |
11 |
67,194,502 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8121:Myh8
|
UTSW |
11 |
67,180,647 (GRCm39) |
missense |
probably benign |
0.00 |
R8125:Myh8
|
UTSW |
11 |
67,190,598 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8170:Myh8
|
UTSW |
11 |
67,179,092 (GRCm39) |
missense |
probably benign |
0.30 |
R8277:Myh8
|
UTSW |
11 |
67,183,735 (GRCm39) |
missense |
probably benign |
0.10 |
R8304:Myh8
|
UTSW |
11 |
67,195,162 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8431:Myh8
|
UTSW |
11 |
67,174,440 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8535:Myh8
|
UTSW |
11 |
67,169,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Myh8
|
UTSW |
11 |
67,174,203 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8858:Myh8
|
UTSW |
11 |
67,192,820 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8928:Myh8
|
UTSW |
11 |
67,174,081 (GRCm39) |
missense |
probably benign |
0.10 |
R9031:Myh8
|
UTSW |
11 |
67,190,141 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9172:Myh8
|
UTSW |
11 |
67,183,260 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9252:Myh8
|
UTSW |
11 |
67,177,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9365:Myh8
|
UTSW |
11 |
67,174,632 (GRCm39) |
missense |
probably benign |
0.42 |
R9468:Myh8
|
UTSW |
11 |
67,197,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
R9565:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
T0722:Myh8
|
UTSW |
11 |
67,195,262 (GRCm39) |
missense |
probably benign |
0.41 |
Z1088:Myh8
|
UTSW |
11 |
67,189,418 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myh8
|
UTSW |
11 |
67,194,500 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myh8
|
UTSW |
11 |
67,199,181 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1177:Myh8
|
UTSW |
11 |
67,192,250 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1187:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1188:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1190:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1191:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
|