Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam10 |
T |
A |
9: 70,661,516 (GRCm39) |
I363N |
probably damaging |
Het |
Ahcyl2 |
T |
C |
6: 29,890,670 (GRCm39) |
|
probably benign |
Het |
Asap1 |
A |
G |
15: 63,966,213 (GRCm39) |
L941P |
probably damaging |
Het |
Aurka |
G |
A |
2: 172,209,067 (GRCm39) |
R23C |
probably benign |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Casp8ap2 |
T |
A |
4: 32,640,381 (GRCm39) |
H478Q |
probably damaging |
Het |
Clcn4 |
C |
T |
7: 7,293,503 (GRCm39) |
A418T |
possibly damaging |
Het |
Cplx3 |
T |
C |
9: 57,521,384 (GRCm39) |
T193A |
probably benign |
Het |
Cpxm2 |
A |
T |
7: 131,645,772 (GRCm39) |
Y715* |
probably null |
Het |
Csmd1 |
T |
C |
8: 16,235,287 (GRCm39) |
M1179V |
probably benign |
Het |
Ddx21 |
A |
T |
10: 62,423,307 (GRCm39) |
F632I |
probably damaging |
Het |
Dnai1 |
C |
A |
4: 41,625,335 (GRCm39) |
T433K |
possibly damaging |
Het |
Dpyd |
G |
A |
3: 119,225,191 (GRCm39) |
G988D |
probably damaging |
Het |
Dync1i2 |
AAAAGAAGAGGAAAGAAGAGGAAAG |
AAAAGAAGAGGAAAG |
2: 71,044,862 (GRCm39) |
|
probably null |
Het |
Dync1li2 |
A |
T |
8: 105,147,297 (GRCm39) |
S466T |
probably benign |
Het |
Ears2 |
T |
C |
7: 121,647,667 (GRCm39) |
T206A |
probably benign |
Het |
Elmod1 |
A |
T |
9: 53,838,876 (GRCm39) |
|
probably benign |
Het |
Eps8l3 |
C |
A |
3: 107,799,661 (GRCm39) |
D590E |
probably benign |
Het |
Etfdh |
A |
T |
3: 79,513,112 (GRCm39) |
H370Q |
probably benign |
Het |
Fam83g |
C |
A |
11: 61,598,489 (GRCm39) |
A792E |
probably benign |
Het |
Ffar3 |
G |
T |
7: 30,554,962 (GRCm39) |
Y119* |
probably null |
Het |
Fosb |
G |
T |
7: 19,041,138 (GRCm39) |
S118R |
possibly damaging |
Het |
Foxn4 |
G |
A |
5: 114,401,175 (GRCm39) |
L3F |
probably damaging |
Het |
Foxo4 |
A |
G |
X: 100,298,784 (GRCm39) |
K65E |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,424,281 (GRCm39) |
L3052P |
probably damaging |
Het |
Fubp3 |
G |
A |
2: 31,498,149 (GRCm39) |
R101H |
probably damaging |
Het |
Gba2 |
C |
A |
4: 43,569,927 (GRCm39) |
G429C |
probably damaging |
Het |
Gimap1 |
T |
C |
6: 48,718,363 (GRCm39) |
|
probably benign |
Het |
Gnas |
A |
G |
2: 174,140,304 (GRCm39) |
T158A |
possibly damaging |
Het |
Gpc5 |
T |
C |
14: 115,789,740 (GRCm39) |
V538A |
probably damaging |
Het |
Greb1l |
T |
C |
18: 10,458,781 (GRCm39) |
|
probably benign |
Het |
H2-M10.5 |
G |
A |
17: 37,085,620 (GRCm39) |
G260R |
probably damaging |
Het |
Hbs1l |
A |
C |
10: 21,225,222 (GRCm39) |
Q412H |
probably benign |
Het |
Hecw1 |
G |
T |
13: 14,411,526 (GRCm39) |
T1058N |
probably damaging |
Het |
Heph |
A |
T |
X: 95,601,690 (GRCm39) |
T1027S |
probably damaging |
Het |
Hoga1 |
A |
C |
19: 42,034,514 (GRCm39) |
E53A |
possibly damaging |
Het |
Insrr |
T |
G |
3: 87,721,744 (GRCm39) |
|
probably benign |
Het |
Ipo11 |
A |
T |
13: 107,028,969 (GRCm39) |
V328D |
probably damaging |
Het |
Jakmip1 |
T |
C |
5: 37,276,217 (GRCm39) |
V509A |
probably damaging |
Het |
Jmjd1c |
T |
C |
10: 67,061,568 (GRCm39) |
V1307A |
probably benign |
Het |
Kmt2a |
T |
A |
9: 44,758,868 (GRCm39) |
S1027C |
probably damaging |
Het |
Kprp |
G |
C |
3: 92,731,664 (GRCm39) |
P462R |
unknown |
Het |
Lrit3 |
A |
T |
3: 129,584,945 (GRCm39) |
V271D |
probably damaging |
Het |
Map4 |
T |
A |
9: 109,808,171 (GRCm39) |
|
probably benign |
Het |
Mark4 |
A |
C |
7: 19,182,598 (GRCm39) |
|
probably benign |
Het |
Mfsd14b |
A |
G |
13: 65,226,259 (GRCm39) |
V142A |
probably benign |
Het |
Mis18bp1 |
A |
T |
12: 65,208,227 (GRCm39) |
I162N |
possibly damaging |
Het |
Mrpl43 |
A |
T |
19: 44,994,391 (GRCm39) |
|
probably benign |
Het |
Mrpl47 |
A |
G |
3: 32,790,842 (GRCm39) |
F16S |
probably benign |
Het |
Myh2 |
G |
T |
11: 67,069,793 (GRCm39) |
G380C |
probably damaging |
Het |
Nectin2 |
A |
G |
7: 19,467,148 (GRCm39) |
|
probably benign |
Het |
Neu3 |
A |
G |
7: 99,463,390 (GRCm39) |
V111A |
probably damaging |
Het |
Nol4l |
T |
C |
2: 153,259,604 (GRCm39) |
|
probably null |
Het |
Nphp3 |
C |
A |
9: 103,900,633 (GRCm39) |
H510Q |
probably damaging |
Het |
Nprl3 |
T |
A |
11: 32,183,118 (GRCm39) |
|
probably null |
Het |
Or14c39 |
A |
G |
7: 86,344,516 (GRCm39) |
N284S |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,674,787 (GRCm39) |
T177A |
probably benign |
Het |
Or52ab7 |
T |
C |
7: 102,978,170 (GRCm39) |
V159A |
probably benign |
Het |
Or6c2 |
T |
C |
10: 129,362,765 (GRCm39) |
I223T |
possibly damaging |
Het |
Pex1 |
A |
G |
5: 3,656,130 (GRCm39) |
E319G |
possibly damaging |
Het |
Pgap6 |
T |
C |
17: 26,336,088 (GRCm39) |
L130S |
probably benign |
Het |
Phtf1 |
C |
A |
3: 103,911,785 (GRCm39) |
T709K |
probably damaging |
Het |
Plek2 |
A |
T |
12: 78,938,946 (GRCm39) |
L271Q |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,191,926 (GRCm39) |
C421* |
probably null |
Het |
Polk |
A |
C |
13: 96,620,687 (GRCm39) |
C525W |
probably damaging |
Het |
Ppfibp2 |
T |
C |
7: 107,328,381 (GRCm39) |
S471P |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,435,546 (GRCm39) |
F74L |
probably benign |
Het |
Prl7d1 |
A |
T |
13: 27,896,038 (GRCm39) |
V113D |
probably benign |
Het |
Prr14 |
C |
T |
7: 127,071,267 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ret |
A |
G |
6: 118,155,571 (GRCm39) |
V375A |
probably damaging |
Het |
Rora |
T |
C |
9: 69,269,028 (GRCm39) |
F41S |
probably damaging |
Het |
Sall1 |
T |
C |
8: 89,758,386 (GRCm39) |
T573A |
probably benign |
Het |
Shb |
A |
G |
4: 45,458,321 (GRCm39) |
V281A |
possibly damaging |
Het |
Slc25a26 |
A |
T |
6: 94,569,391 (GRCm39) |
|
probably null |
Het |
Sltm |
T |
C |
9: 70,493,363 (GRCm39) |
F769L |
probably damaging |
Het |
Snx9 |
T |
A |
17: 5,968,688 (GRCm39) |
M328K |
probably damaging |
Het |
Stk25 |
G |
T |
1: 93,552,313 (GRCm39) |
Q356K |
probably benign |
Het |
Svep1 |
T |
A |
4: 58,128,858 (GRCm39) |
Y613F |
possibly damaging |
Het |
Syne4 |
G |
A |
7: 30,016,169 (GRCm39) |
A195T |
probably damaging |
Het |
Tmem217b |
A |
T |
17: 29,738,545 (GRCm39) |
F74I |
probably benign |
Het |
Trcg1 |
C |
T |
9: 57,149,616 (GRCm39) |
T396M |
probably damaging |
Het |
Trim30b |
A |
G |
7: 104,006,505 (GRCm39) |
V117A |
possibly damaging |
Het |
Trpc4 |
T |
C |
3: 54,209,511 (GRCm39) |
|
probably benign |
Het |
Ttll4 |
A |
G |
1: 74,727,439 (GRCm39) |
H827R |
probably damaging |
Het |
Tut7 |
A |
G |
13: 59,948,131 (GRCm39) |
V328A |
probably benign |
Het |
Urgcp |
T |
C |
11: 5,667,477 (GRCm39) |
E287G |
probably damaging |
Het |
Usp2 |
G |
T |
9: 44,004,081 (GRCm39) |
L319F |
probably damaging |
Het |
Vmn1r167 |
A |
T |
7: 23,204,512 (GRCm39) |
V168D |
probably damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
Vmn2r61 |
A |
T |
7: 41,915,442 (GRCm39) |
I130F |
probably benign |
Het |
Vmn2r63 |
A |
T |
7: 42,577,952 (GRCm39) |
Y195* |
probably null |
Het |
Vmn2r81 |
T |
C |
10: 79,129,283 (GRCm39) |
S725P |
probably damaging |
Het |
Wnt10b |
A |
G |
15: 98,670,818 (GRCm39) |
|
probably benign |
Het |
Zfp292 |
T |
C |
4: 34,807,194 (GRCm39) |
E1950G |
probably damaging |
Het |
Zfyve16 |
A |
G |
13: 92,653,028 (GRCm39) |
|
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 |
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 |
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 |
|