Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
T |
C |
2: 152,283,161 (GRCm39) |
I275T |
probably benign |
Het |
Chd9 |
A |
T |
8: 91,683,122 (GRCm39) |
K521* |
probably null |
Het |
Csn3 |
A |
T |
5: 88,077,956 (GRCm39) |
N154I |
possibly damaging |
Het |
Dock2 |
A |
G |
11: 34,180,670 (GRCm39) |
S1716P |
probably benign |
Het |
Dock7 |
A |
T |
4: 98,846,304 (GRCm39) |
S18T |
probably benign |
Het |
Esrra |
G |
A |
19: 6,891,190 (GRCm39) |
T190I |
probably benign |
Het |
F13b |
T |
C |
1: 139,444,115 (GRCm39) |
I483T |
probably damaging |
Het |
Foxb1 |
T |
A |
9: 69,666,985 (GRCm39) |
M182L |
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,809,065 (GRCm39) |
F1795L |
probably benign |
Het |
Gkn2 |
G |
A |
6: 87,350,390 (GRCm39) |
|
probably null |
Het |
Gm8439 |
G |
A |
4: 120,466,787 (GRCm39) |
A93T |
unknown |
Het |
Ift22 |
T |
C |
5: 136,940,550 (GRCm39) |
S72P |
probably benign |
Het |
Kcnmb2 |
A |
G |
3: 32,232,993 (GRCm39) |
K24E |
probably damaging |
Het |
Kcnq3 |
C |
A |
15: 65,897,040 (GRCm39) |
V287L |
probably damaging |
Het |
Lrriq1 |
T |
A |
10: 103,006,340 (GRCm39) |
M1262L |
probably benign |
Het |
Mb21d2 |
A |
G |
16: 28,748,240 (GRCm39) |
I59T |
probably benign |
Het |
Mogat2 |
A |
T |
7: 98,872,761 (GRCm39) |
M141K |
possibly damaging |
Het |
Mtdh |
C |
T |
15: 34,131,396 (GRCm39) |
L409F |
possibly damaging |
Het |
Muc5ac |
C |
T |
7: 141,372,537 (GRCm39) |
Q2724* |
probably null |
Het |
Nodal |
C |
T |
10: 61,260,324 (GRCm39) |
T325I |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,215,674 (GRCm39) |
T1194S |
probably damaging |
Het |
Pcdhb13 |
A |
C |
18: 37,576,738 (GRCm39) |
D372A |
probably damaging |
Het |
Phf14 |
T |
A |
6: 11,934,015 (GRCm39) |
N292K |
probably damaging |
Het |
Pigr |
T |
A |
1: 130,776,793 (GRCm39) |
|
probably null |
Het |
Plcb1 |
T |
C |
2: 135,229,773 (GRCm39) |
I1131T |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,688,772 (GRCm39) |
D132V |
probably damaging |
Het |
Plxnb2 |
C |
A |
15: 89,050,016 (GRCm39) |
E502* |
probably null |
Het |
Prox2 |
T |
C |
12: 85,134,703 (GRCm39) |
N526S |
probably damaging |
Het |
Rdm1 |
T |
A |
11: 101,519,280 (GRCm39) |
|
probably null |
Het |
Rxfp1 |
C |
T |
3: 79,567,427 (GRCm39) |
E308K |
probably benign |
Het |
Sgca |
T |
C |
11: 94,854,110 (GRCm39) |
T120A |
probably damaging |
Het |
Sh3tc1 |
G |
A |
5: 35,860,696 (GRCm39) |
R1054W |
probably damaging |
Het |
Smarcal1 |
C |
T |
1: 72,672,214 (GRCm39) |
|
probably benign |
Het |
Spata45 |
T |
A |
1: 190,771,958 (GRCm39) |
M60K |
probably benign |
Het |
St8sia6 |
T |
C |
2: 13,661,716 (GRCm39) |
M372V |
probably damaging |
Het |
Tas2r126 |
T |
G |
6: 42,411,598 (GRCm39) |
S44A |
probably benign |
Het |
Tcea3 |
T |
A |
4: 136,000,945 (GRCm39) |
|
probably benign |
Het |
Thoc2l |
A |
G |
5: 104,668,949 (GRCm39) |
E1157G |
probably benign |
Het |
Tln1 |
T |
C |
4: 43,546,857 (GRCm39) |
I840V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,728,685 (GRCm39) |
|
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,187,471 (GRCm39) |
Y3846* |
probably null |
Het |
Usp47 |
G |
A |
7: 111,703,256 (GRCm39) |
D1171N |
probably benign |
Het |
Vmn2r114 |
G |
A |
17: 23,510,782 (GRCm39) |
T566I |
probably benign |
Het |
Wdr35 |
G |
A |
12: 9,058,535 (GRCm39) |
R575Q |
probably null |
Het |
Xkr5 |
A |
T |
8: 18,983,683 (GRCm39) |
C454S |
probably benign |
Het |
|
Other mutations in Myo15a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00845:Myo15a
|
APN |
11 |
60,368,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Myo15a
|
APN |
11 |
60,367,818 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01100:Myo15a
|
APN |
11 |
60,401,984 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01357:Myo15a
|
APN |
11 |
60,393,115 (GRCm39) |
splice site |
probably benign |
|
IGL01634:Myo15a
|
APN |
11 |
60,386,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01763:Myo15a
|
APN |
11 |
60,412,564 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01901:Myo15a
|
APN |
11 |
60,418,260 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01931:Myo15a
|
APN |
11 |
60,386,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02006:Myo15a
|
APN |
11 |
60,401,954 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02041:Myo15a
|
APN |
11 |
60,397,689 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02094:Myo15a
|
APN |
11 |
60,401,473 (GRCm39) |
unclassified |
probably benign |
|
IGL02122:Myo15a
|
APN |
11 |
60,374,292 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02328:Myo15a
|
APN |
11 |
60,417,433 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02330:Myo15a
|
APN |
11 |
60,367,987 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02431:Myo15a
|
APN |
11 |
60,401,465 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02639:Myo15a
|
APN |
11 |
60,369,447 (GRCm39) |
missense |
probably benign |
|
IGL02659:Myo15a
|
APN |
11 |
60,382,609 (GRCm39) |
splice site |
probably benign |
|
IGL02800:Myo15a
|
APN |
11 |
60,393,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Myo15a
|
APN |
11 |
60,368,005 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02863:Myo15a
|
APN |
11 |
60,368,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02873:Myo15a
|
APN |
11 |
60,374,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02990:Myo15a
|
APN |
11 |
60,370,266 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03011:Myo15a
|
APN |
11 |
60,400,357 (GRCm39) |
splice site |
probably benign |
|
IGL03243:Myo15a
|
APN |
11 |
60,387,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Myo15a
|
APN |
11 |
60,369,967 (GRCm39) |
missense |
probably damaging |
1.00 |
novichok
|
UTSW |
11 |
60,372,566 (GRCm39) |
critical splice donor site |
probably null |
|
parker
|
UTSW |
11 |
60,411,740 (GRCm39) |
critical splice donor site |
probably null |
|
Typhoon
|
UTSW |
11 |
60,378,251 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4131001:Myo15a
|
UTSW |
11 |
60,386,280 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Myo15a
|
UTSW |
11 |
60,373,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Myo15a
|
UTSW |
11 |
60,368,676 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0265:Myo15a
|
UTSW |
11 |
60,405,723 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0389:Myo15a
|
UTSW |
11 |
60,369,364 (GRCm39) |
missense |
probably benign |
|
R0416:Myo15a
|
UTSW |
11 |
60,402,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Myo15a
|
UTSW |
11 |
60,400,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0477:Myo15a
|
UTSW |
11 |
60,411,740 (GRCm39) |
critical splice donor site |
probably null |
|
R0543:Myo15a
|
UTSW |
11 |
60,369,877 (GRCm39) |
missense |
probably benign |
|
R0546:Myo15a
|
UTSW |
11 |
60,397,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Myo15a
|
UTSW |
11 |
60,412,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0639:Myo15a
|
UTSW |
11 |
60,370,162 (GRCm39) |
missense |
probably benign |
0.12 |
R0723:Myo15a
|
UTSW |
11 |
60,369,803 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0837:Myo15a
|
UTSW |
11 |
60,378,077 (GRCm39) |
missense |
probably damaging |
0.98 |
R0865:Myo15a
|
UTSW |
11 |
60,382,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R0899:Myo15a
|
UTSW |
11 |
60,368,011 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1022:Myo15a
|
UTSW |
11 |
60,370,442 (GRCm39) |
missense |
probably benign |
0.00 |
R1024:Myo15a
|
UTSW |
11 |
60,370,442 (GRCm39) |
missense |
probably benign |
0.00 |
R1035:Myo15a
|
UTSW |
11 |
60,401,384 (GRCm39) |
unclassified |
probably benign |
|
R1109:Myo15a
|
UTSW |
11 |
60,383,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Myo15a
|
UTSW |
11 |
60,370,233 (GRCm39) |
missense |
probably benign |
0.04 |
R1241:Myo15a
|
UTSW |
11 |
60,390,256 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1392:Myo15a
|
UTSW |
11 |
60,368,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1392:Myo15a
|
UTSW |
11 |
60,368,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1434:Myo15a
|
UTSW |
11 |
60,395,157 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Myo15a
|
UTSW |
11 |
60,386,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Myo15a
|
UTSW |
11 |
60,399,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Myo15a
|
UTSW |
11 |
60,379,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R1551:Myo15a
|
UTSW |
11 |
60,383,791 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1571:Myo15a
|
UTSW |
11 |
60,409,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Myo15a
|
UTSW |
11 |
60,392,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Myo15a
|
UTSW |
11 |
60,405,762 (GRCm39) |
missense |
probably benign |
|
R1778:Myo15a
|
UTSW |
11 |
60,369,238 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1847:Myo15a
|
UTSW |
11 |
60,390,321 (GRCm39) |
nonsense |
probably null |
|
R1875:Myo15a
|
UTSW |
11 |
60,398,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R1944:Myo15a
|
UTSW |
11 |
60,392,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R1945:Myo15a
|
UTSW |
11 |
60,392,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R2013:Myo15a
|
UTSW |
11 |
60,385,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Myo15a
|
UTSW |
11 |
60,382,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Myo15a
|
UTSW |
11 |
60,382,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Myo15a
|
UTSW |
11 |
60,384,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R2147:Myo15a
|
UTSW |
11 |
60,401,055 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2196:Myo15a
|
UTSW |
11 |
60,400,847 (GRCm39) |
nonsense |
probably null |
|
R2207:Myo15a
|
UTSW |
11 |
60,396,860 (GRCm39) |
missense |
probably benign |
0.01 |
R2245:Myo15a
|
UTSW |
11 |
60,399,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Myo15a
|
UTSW |
11 |
60,408,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R2374:Myo15a
|
UTSW |
11 |
60,369,669 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2438:Myo15a
|
UTSW |
11 |
60,373,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Myo15a
|
UTSW |
11 |
60,370,186 (GRCm39) |
splice site |
probably null |
|
R3423:Myo15a
|
UTSW |
11 |
60,401,126 (GRCm39) |
critical splice donor site |
probably null |
|
R3551:Myo15a
|
UTSW |
11 |
60,400,489 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3552:Myo15a
|
UTSW |
11 |
60,400,489 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3612:Myo15a
|
UTSW |
11 |
60,368,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R3620:Myo15a
|
UTSW |
11 |
60,369,468 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3713:Myo15a
|
UTSW |
11 |
60,370,057 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3714:Myo15a
|
UTSW |
11 |
60,370,057 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3715:Myo15a
|
UTSW |
11 |
60,370,057 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3783:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3784:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3785:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3786:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3787:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3894:Myo15a
|
UTSW |
11 |
60,395,145 (GRCm39) |
missense |
probably benign |
0.00 |
R3962:Myo15a
|
UTSW |
11 |
60,370,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4082:Myo15a
|
UTSW |
11 |
60,378,022 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4555:Myo15a
|
UTSW |
11 |
60,387,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Myo15a
|
UTSW |
11 |
60,393,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Myo15a
|
UTSW |
11 |
60,395,705 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4713:Myo15a
|
UTSW |
11 |
60,370,756 (GRCm39) |
missense |
probably benign |
0.21 |
R4820:Myo15a
|
UTSW |
11 |
60,367,741 (GRCm39) |
missense |
probably damaging |
0.98 |
R5013:Myo15a
|
UTSW |
11 |
60,382,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5051:Myo15a
|
UTSW |
11 |
60,378,251 (GRCm39) |
critical splice donor site |
probably null |
|
R5187:Myo15a
|
UTSW |
11 |
60,394,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Myo15a
|
UTSW |
11 |
60,393,674 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5277:Myo15a
|
UTSW |
11 |
60,367,940 (GRCm39) |
nonsense |
probably null |
|
R5345:Myo15a
|
UTSW |
11 |
60,388,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R5349:Myo15a
|
UTSW |
11 |
60,384,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Myo15a
|
UTSW |
11 |
60,389,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Myo15a
|
UTSW |
11 |
60,411,603 (GRCm39) |
nonsense |
probably null |
|
R5477:Myo15a
|
UTSW |
11 |
60,368,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Myo15a
|
UTSW |
11 |
60,370,578 (GRCm39) |
missense |
probably benign |
|
R5728:Myo15a
|
UTSW |
11 |
60,379,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5818:Myo15a
|
UTSW |
11 |
60,388,777 (GRCm39) |
missense |
probably benign |
0.06 |
R5952:Myo15a
|
UTSW |
11 |
60,370,246 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6338:Myo15a
|
UTSW |
11 |
60,368,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R6467:Myo15a
|
UTSW |
11 |
60,417,487 (GRCm39) |
critical splice donor site |
probably null |
|
R6488:Myo15a
|
UTSW |
11 |
60,369,313 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6521:Myo15a
|
UTSW |
11 |
60,393,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Myo15a
|
UTSW |
11 |
60,368,118 (GRCm39) |
missense |
probably benign |
0.00 |
R6702:Myo15a
|
UTSW |
11 |
60,383,818 (GRCm39) |
missense |
probably benign |
0.16 |
R6703:Myo15a
|
UTSW |
11 |
60,383,818 (GRCm39) |
missense |
probably benign |
0.16 |
R6821:Myo15a
|
UTSW |
11 |
60,415,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Myo15a
|
UTSW |
11 |
60,414,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6932:Myo15a
|
UTSW |
11 |
60,390,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R6958:Myo15a
|
UTSW |
11 |
60,394,451 (GRCm39) |
missense |
probably benign |
0.07 |
R7041:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Myo15a
|
UTSW |
11 |
60,400,836 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7163:Myo15a
|
UTSW |
11 |
60,389,195 (GRCm39) |
missense |
|
|
R7229:Myo15a
|
UTSW |
11 |
60,387,321 (GRCm39) |
missense |
probably benign |
0.08 |
R7347:Myo15a
|
UTSW |
11 |
60,368,787 (GRCm39) |
missense |
probably benign |
|
R7368:Myo15a
|
UTSW |
11 |
60,381,741 (GRCm39) |
splice site |
probably null |
|
R7392:Myo15a
|
UTSW |
11 |
60,396,802 (GRCm39) |
missense |
|
|
R7414:Myo15a
|
UTSW |
11 |
60,374,309 (GRCm39) |
missense |
|
|
R7461:Myo15a
|
UTSW |
11 |
60,395,978 (GRCm39) |
missense |
|
|
R7609:Myo15a
|
UTSW |
11 |
60,379,637 (GRCm39) |
missense |
|
|
R7613:Myo15a
|
UTSW |
11 |
60,395,978 (GRCm39) |
missense |
|
|
R7734:Myo15a
|
UTSW |
11 |
60,401,108 (GRCm39) |
missense |
probably benign |
|
R7748:Myo15a
|
UTSW |
11 |
60,395,727 (GRCm39) |
missense |
|
|
R7767:Myo15a
|
UTSW |
11 |
60,392,922 (GRCm39) |
missense |
|
|
R7769:Myo15a
|
UTSW |
11 |
60,399,975 (GRCm39) |
missense |
|
|
R7894:Myo15a
|
UTSW |
11 |
60,381,963 (GRCm39) |
missense |
|
|
R7919:Myo15a
|
UTSW |
11 |
60,417,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R8100:Myo15a
|
UTSW |
11 |
60,408,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Myo15a
|
UTSW |
11 |
60,398,279 (GRCm39) |
missense |
|
|
R8129:Myo15a
|
UTSW |
11 |
60,399,026 (GRCm39) |
missense |
|
|
R8428:Myo15a
|
UTSW |
11 |
60,387,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8706:Myo15a
|
UTSW |
11 |
60,370,443 (GRCm39) |
missense |
probably benign |
|
R8735:Myo15a
|
UTSW |
11 |
60,401,679 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8739:Myo15a
|
UTSW |
11 |
60,368,088 (GRCm39) |
missense |
probably benign |
0.06 |
R8790:Myo15a
|
UTSW |
11 |
60,378,047 (GRCm39) |
missense |
|
|
R8790:Myo15a
|
UTSW |
11 |
60,367,362 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8822:Myo15a
|
UTSW |
11 |
60,367,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R8907:Myo15a
|
UTSW |
11 |
60,417,434 (GRCm39) |
missense |
|
|
R8931:Myo15a
|
UTSW |
11 |
60,368,020 (GRCm39) |
missense |
probably benign |
|
R9061:Myo15a
|
UTSW |
11 |
60,393,692 (GRCm39) |
missense |
|
|
R9124:Myo15a
|
UTSW |
11 |
60,369,952 (GRCm39) |
missense |
probably benign |
0.37 |
R9297:Myo15a
|
UTSW |
11 |
60,385,899 (GRCm39) |
missense |
probably null |
|
R9347:Myo15a
|
UTSW |
11 |
60,374,555 (GRCm39) |
missense |
|
|
R9417:Myo15a
|
UTSW |
11 |
60,378,243 (GRCm39) |
missense |
|
|
R9456:Myo15a
|
UTSW |
11 |
60,392,668 (GRCm39) |
missense |
|
|
R9460:Myo15a
|
UTSW |
11 |
60,372,566 (GRCm39) |
critical splice donor site |
probably null |
|
R9615:Myo15a
|
UTSW |
11 |
60,374,320 (GRCm39) |
missense |
|
|
R9630:Myo15a
|
UTSW |
11 |
60,407,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9746:Myo15a
|
UTSW |
11 |
60,378,234 (GRCm39) |
nonsense |
probably null |
|
X0021:Myo15a
|
UTSW |
11 |
60,373,185 (GRCm39) |
nonsense |
probably null |
|
X0066:Myo15a
|
UTSW |
11 |
60,369,046 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Myo15a
|
UTSW |
11 |
60,369,444 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Myo15a
|
UTSW |
11 |
60,389,229 (GRCm39) |
missense |
|
|
Z1176:Myo15a
|
UTSW |
11 |
60,379,084 (GRCm39) |
missense |
|
|
Z1176:Myo15a
|
UTSW |
11 |
60,415,267 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo15a
|
UTSW |
11 |
60,386,301 (GRCm39) |
missense |
|
|
Z1177:Myo15a
|
UTSW |
11 |
60,379,663 (GRCm39) |
missense |
|
|
Z1177:Myo15a
|
UTSW |
11 |
60,368,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|