Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anxa2 |
T |
C |
9: 69,398,764 (GRCm39) |
Y333H |
probably benign |
Het |
Arid1a |
A |
T |
4: 133,408,679 (GRCm39) |
F1558I |
unknown |
Het |
Aste1 |
A |
G |
9: 105,274,678 (GRCm39) |
D306G |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,596,590 (GRCm39) |
V843A |
possibly damaging |
Het |
Atrip |
T |
A |
9: 108,894,574 (GRCm39) |
H451L |
probably benign |
Het |
Cdc42bpb |
T |
C |
12: 111,295,664 (GRCm39) |
D200G |
probably damaging |
Het |
Ceacam19 |
A |
C |
7: 19,620,520 (GRCm39) |
M37R |
probably benign |
Het |
Cemip |
G |
A |
7: 83,606,872 (GRCm39) |
R782* |
probably null |
Het |
Cpe |
A |
T |
8: 65,070,654 (GRCm39) |
I197N |
probably benign |
Het |
Csmd2 |
C |
A |
4: 128,445,850 (GRCm39) |
P3307T |
|
Het |
Cyp4a12b |
C |
A |
4: 115,268,937 (GRCm39) |
Q20K |
possibly damaging |
Het |
Dcaf1 |
T |
C |
9: 106,715,878 (GRCm39) |
Y332H |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,298,163 (GRCm39) |
H569R |
probably damaging |
Het |
Dcp1b |
A |
G |
6: 119,192,244 (GRCm39) |
S387G |
probably benign |
Het |
Ddx24 |
A |
G |
12: 103,383,819 (GRCm39) |
M590T |
possibly damaging |
Het |
Dixdc1 |
T |
G |
9: 50,613,268 (GRCm39) |
Q229P |
probably damaging |
Het |
Dnase1l3 |
T |
C |
14: 7,977,144 (GRCm38) |
R181G |
probably benign |
Het |
Dzip1l |
A |
T |
9: 99,549,735 (GRCm39) |
D735V |
probably damaging |
Het |
Edem3 |
T |
C |
1: 151,694,336 (GRCm39) |
S890P |
probably benign |
Het |
Fuom |
A |
G |
7: 139,679,455 (GRCm39) |
L155P |
unknown |
Het |
Gm6408 |
C |
A |
5: 146,421,160 (GRCm39) |
S263* |
probably null |
Het |
Helz |
C |
G |
11: 107,576,248 (GRCm39) |
S1814R |
unknown |
Het |
Hrc |
T |
C |
7: 44,986,100 (GRCm39) |
L417P |
probably benign |
Het |
Igdcc4 |
A |
C |
9: 65,039,035 (GRCm39) |
H894P |
probably damaging |
Het |
Lgr6 |
C |
A |
1: 134,930,981 (GRCm39) |
V296L |
probably damaging |
Het |
Map3k4 |
T |
A |
17: 12,482,998 (GRCm39) |
Y573F |
probably damaging |
Het |
Mest |
T |
C |
6: 30,746,299 (GRCm39) |
Y296H |
unknown |
Het |
Mettl21a |
C |
T |
1: 64,647,288 (GRCm39) |
V90M |
probably damaging |
Het |
Mfsd4b1 |
A |
T |
10: 39,883,374 (GRCm39) |
N25K |
probably damaging |
Het |
Mmd |
T |
A |
11: 90,167,579 (GRCm39) |
F203I |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 70,998,826 (GRCm39) |
N859I |
unknown |
Het |
Nrcam |
T |
C |
12: 44,584,034 (GRCm39) |
L36P |
possibly damaging |
Het |
Nup107 |
C |
A |
10: 117,593,917 (GRCm39) |
E759* |
probably null |
Het |
Or14a259 |
A |
G |
7: 86,013,476 (GRCm39) |
I23T |
not run |
Het |
Pcdh7 |
T |
G |
5: 57,876,976 (GRCm39) |
I177S |
probably damaging |
Het |
Pde6a |
T |
C |
18: 61,365,938 (GRCm39) |
I221T |
probably benign |
Het |
Ptpn13 |
A |
T |
5: 103,709,828 (GRCm39) |
N1497I |
probably damaging |
Het |
Rmc1 |
T |
A |
18: 12,322,320 (GRCm39) |
I591N |
possibly damaging |
Het |
Rpl4 |
T |
A |
9: 64,084,661 (GRCm39) |
H245Q |
probably benign |
Het |
Rsf1 |
C |
CCACGGCGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Scara5 |
A |
G |
14: 65,968,600 (GRCm39) |
D291G |
possibly damaging |
Het |
Septin14 |
T |
A |
5: 129,760,583 (GRCm39) |
I422L |
probably benign |
Het |
Serpina1e |
T |
C |
12: 103,917,151 (GRCm39) |
K173E |
probably benign |
Het |
Slc5a1 |
C |
T |
5: 33,318,279 (GRCm39) |
T644I |
probably benign |
Het |
Slc6a13 |
A |
T |
6: 121,314,334 (GRCm39) |
T590S |
probably benign |
Het |
Smarca4 |
C |
T |
9: 21,578,658 (GRCm39) |
T938I |
possibly damaging |
Het |
Stxbp1 |
A |
T |
2: 32,691,832 (GRCm39) |
D453E |
probably benign |
Het |
Tcf12 |
C |
A |
9: 71,829,943 (GRCm39) |
V173L |
probably benign |
Het |
Tenm3 |
A |
G |
8: 49,099,368 (GRCm39) |
C146R |
probably damaging |
Het |
Trim11 |
T |
C |
11: 58,869,180 (GRCm39) |
C39R |
probably damaging |
Het |
Trim37 |
A |
G |
11: 87,068,821 (GRCm39) |
Y389C |
probably damaging |
Het |
Ttll8 |
C |
T |
15: 88,798,368 (GRCm39) |
G789D |
probably damaging |
Het |
Tubb2a |
C |
T |
13: 34,258,776 (GRCm39) |
S338N |
probably benign |
Het |
Ulk2 |
G |
A |
11: 61,744,127 (GRCm39) |
Q50* |
probably null |
Het |
Urgcp |
T |
C |
11: 5,666,406 (GRCm39) |
D687G |
probably benign |
Het |
Usp13 |
C |
T |
3: 32,892,054 (GRCm39) |
H78Y |
probably benign |
Het |
Vmn2r100 |
T |
A |
17: 19,742,296 (GRCm39) |
D223E |
probably benign |
Het |
Vwc2 |
G |
A |
11: 11,065,929 (GRCm39) |
A6T |
possibly damaging |
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 |
IGL02153:Myo15a
|
APN |
11 |
60,389,223 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|
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 |
|