Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
T |
A |
7: 130,963,521 (GRCm39) |
L103F |
probably benign |
Het |
5330417H12Rik |
A |
G |
7: 107,223,765 (GRCm39) |
L103P |
unknown |
Het |
Actb |
T |
C |
5: 142,890,450 (GRCm39) |
I151V |
probably benign |
Het |
Adcy6 |
T |
A |
15: 98,502,437 (GRCm39) |
H59L |
probably benign |
Het |
Adss2 |
G |
C |
1: 177,599,768 (GRCm39) |
S272* |
probably null |
Het |
Aga |
A |
T |
8: 53,964,840 (GRCm39) |
M1L |
possibly damaging |
Het |
Ajm1 |
T |
A |
2: 25,468,971 (GRCm39) |
E313D |
possibly damaging |
Het |
Anxa5 |
G |
A |
3: 36,519,480 (GRCm39) |
T3M |
probably damaging |
Het |
Arhgap45 |
A |
T |
10: 79,852,766 (GRCm39) |
|
probably benign |
Het |
Atp6v0a2 |
A |
T |
5: 124,793,560 (GRCm39) |
H639L |
probably benign |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Bcl2l2 |
C |
T |
14: 55,121,836 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,013,484 (GRCm39) |
|
probably null |
Het |
Bod1l |
A |
C |
5: 41,989,683 (GRCm39) |
S347A |
probably damaging |
Het |
Calcoco1 |
T |
C |
15: 102,627,996 (GRCm39) |
D46G |
probably damaging |
Het |
Camk1 |
T |
C |
6: 113,317,289 (GRCm39) |
E60G |
probably damaging |
Het |
Capza1 |
A |
T |
3: 104,732,721 (GRCm39) |
|
probably null |
Het |
Ccdc18 |
T |
A |
5: 108,296,907 (GRCm39) |
|
probably null |
Het |
Cdh20 |
G |
A |
1: 104,869,024 (GRCm39) |
A172T |
probably damaging |
Het |
Cdk4 |
C |
T |
10: 126,900,298 (GRCm39) |
A65V |
possibly damaging |
Het |
Cftr |
T |
C |
6: 18,277,888 (GRCm39) |
|
probably null |
Het |
Chd3 |
T |
C |
11: 69,246,459 (GRCm39) |
M1092V |
probably benign |
Het |
Chd6 |
A |
T |
2: 160,808,539 (GRCm39) |
H1558Q |
probably benign |
Het |
Chi3l1 |
A |
G |
1: 134,116,966 (GRCm39) |
H318R |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,178,965 (GRCm39) |
Y59C |
probably damaging |
Het |
Cyb5r4 |
T |
C |
9: 86,914,434 (GRCm39) |
V111A |
probably damaging |
Het |
Ddx39b |
G |
A |
17: 35,471,726 (GRCm39) |
V291M |
probably damaging |
Het |
Dhx57 |
A |
G |
17: 80,572,546 (GRCm39) |
F709S |
probably damaging |
Het |
Eef1b2 |
A |
T |
1: 63,217,024 (GRCm39) |
K64N |
probably damaging |
Het |
Eef1ece2 |
A |
T |
16: 20,451,834 (GRCm39) |
D407V |
probably damaging |
Het |
Fam135a |
A |
G |
1: 24,068,050 (GRCm39) |
S940P |
probably benign |
Het |
Fam234b |
T |
A |
6: 135,186,349 (GRCm39) |
V119E |
probably damaging |
Het |
Fbxo46 |
G |
C |
7: 18,870,458 (GRCm39) |
C359S |
probably damaging |
Het |
Fkbp14 |
C |
A |
6: 54,572,505 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
T |
A |
1: 174,494,215 (GRCm39) |
V1243E |
probably damaging |
Het |
Fsbp |
C |
A |
4: 11,579,924 (GRCm39) |
T64K |
probably damaging |
Het |
Fscb |
A |
T |
12: 64,521,181 (GRCm39) |
M95K |
probably benign |
Het |
Fyb1 |
T |
G |
15: 6,668,307 (GRCm39) |
V500G |
probably damaging |
Het |
G2e3 |
A |
G |
12: 51,418,450 (GRCm39) |
N615S |
probably benign |
Het |
Gart |
T |
C |
16: 91,427,540 (GRCm39) |
D486G |
possibly damaging |
Het |
Gas2l2 |
T |
A |
11: 83,313,224 (GRCm39) |
D696V |
probably benign |
Het |
Glmn |
C |
T |
5: 107,710,110 (GRCm39) |
|
probably null |
Het |
Gm47985 |
A |
T |
1: 151,058,725 (GRCm39) |
D122V |
probably damaging |
Het |
Gm7168 |
A |
G |
17: 14,168,914 (GRCm39) |
K94E |
probably benign |
Het |
Gnai2 |
T |
C |
9: 107,492,934 (GRCm39) |
H323R |
|
Het |
Helz2 |
C |
T |
2: 180,876,324 (GRCm39) |
R1390H |
probably damaging |
Het |
Igf2bp1 |
T |
C |
11: 95,858,413 (GRCm39) |
M453V |
probably benign |
Het |
Ighv3-1 |
C |
T |
12: 113,928,270 (GRCm39) |
V30M |
probably damaging |
Het |
Inpp5a |
A |
T |
7: 139,154,911 (GRCm39) |
R343S |
probably damaging |
Het |
Itga8 |
T |
A |
2: 12,235,050 (GRCm39) |
I403F |
possibly damaging |
Het |
Katnip |
A |
T |
7: 125,428,973 (GRCm39) |
M558L |
probably benign |
Het |
Krt33a |
C |
T |
11: 99,902,428 (GRCm39) |
R404H |
probably benign |
Het |
Krt34 |
T |
A |
11: 99,929,764 (GRCm39) |
E244V |
probably damaging |
Het |
Krt42 |
T |
C |
11: 100,157,792 (GRCm39) |
E224G |
probably damaging |
Het |
Krtap5-2 |
TCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACCACAGCCCCCACAGGAACTACA |
TCCACAGGAACTACA |
7: 141,728,845 (GRCm39) |
|
probably benign |
Het |
Lama1 |
T |
C |
17: 68,057,585 (GRCm39) |
L553P |
|
Het |
Lcn9 |
T |
A |
2: 25,714,926 (GRCm39) |
*179K |
probably null |
Het |
Ldaf1 |
A |
T |
7: 119,714,702 (GRCm39) |
I64F |
possibly damaging |
Het |
Lrrc2 |
T |
G |
9: 110,809,999 (GRCm39) |
M345R |
possibly damaging |
Het |
Marchf11 |
T |
C |
15: 26,387,916 (GRCm39) |
V257A |
probably damaging |
Het |
Masp2 |
T |
C |
4: 148,690,163 (GRCm39) |
I224T |
probably benign |
Het |
Mpz |
A |
T |
1: 170,987,509 (GRCm39) |
|
probably null |
Het |
Mtr |
C |
T |
13: 12,242,725 (GRCm39) |
A442T |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,401,542 (GRCm39) |
K596R |
unknown |
Het |
Ncor2 |
T |
C |
5: 125,187,031 (GRCm39) |
I173V |
unknown |
Het |
Ngly1 |
T |
A |
14: 16,290,820 (GRCm38) |
I434K |
possibly damaging |
Het |
Notch2 |
A |
G |
3: 98,045,800 (GRCm39) |
H1655R |
possibly damaging |
Het |
Notum |
C |
T |
11: 120,545,627 (GRCm39) |
A390T |
probably damaging |
Het |
Or10a3n |
T |
C |
7: 108,493,285 (GRCm39) |
T115A |
probably benign |
Het |
Or1e22 |
T |
G |
11: 73,376,994 (GRCm39) |
I219L |
probably benign |
Het |
Pds5a |
T |
A |
5: 65,777,009 (GRCm39) |
I51F |
possibly damaging |
Het |
Pdzd2 |
C |
A |
15: 12,385,872 (GRCm39) |
R966L |
possibly damaging |
Het |
Plk3 |
T |
C |
4: 116,988,925 (GRCm39) |
Y278C |
probably damaging |
Het |
Plxna1 |
C |
G |
6: 89,314,334 (GRCm39) |
|
probably null |
Het |
Plxna1 |
T |
A |
6: 89,314,335 (GRCm39) |
|
probably null |
Het |
Ppp4r4 |
G |
A |
12: 103,571,320 (GRCm39) |
|
probably null |
Het |
Pramel6 |
T |
A |
2: 87,339,043 (GRCm39) |
V81E |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,862,459 (GRCm39) |
E277G |
possibly damaging |
Het |
Prkg1 |
T |
A |
19: 30,970,491 (GRCm39) |
I222F |
possibly damaging |
Het |
Proser3 |
A |
T |
7: 30,239,497 (GRCm39) |
S536T |
possibly damaging |
Het |
Prrt4 |
C |
A |
6: 29,177,190 (GRCm39) |
G193V |
probably damaging |
Het |
Ptpn21 |
A |
T |
12: 98,655,031 (GRCm39) |
H645Q |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,017,741 (GRCm39) |
I744V |
probably null |
Het |
Rad54l2 |
A |
G |
9: 106,596,233 (GRCm39) |
V235A |
possibly damaging |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Rgs22 |
C |
T |
15: 36,122,415 (GRCm39) |
|
probably null |
Het |
Rtcb |
A |
T |
10: 85,777,832 (GRCm39) |
D447E |
probably benign |
Het |
Rtn1 |
C |
T |
12: 72,263,700 (GRCm39) |
V744I |
possibly damaging |
Het |
Scfd1 |
T |
G |
12: 51,436,140 (GRCm39) |
I96M |
probably benign |
Het |
Serpina3b |
T |
C |
12: 104,096,722 (GRCm39) |
M1T |
probably null |
Het |
Slc1a4 |
T |
C |
11: 20,282,252 (GRCm39) |
Y74C |
probably damaging |
Het |
Slc9b2 |
A |
T |
3: 135,031,940 (GRCm39) |
I267F |
possibly damaging |
Het |
Sorcs2 |
A |
T |
5: 36,386,519 (GRCm39) |
M173K |
possibly damaging |
Het |
Sparc |
T |
C |
11: 55,289,426 (GRCm39) |
I226V |
probably benign |
Het |
Spata22 |
T |
G |
11: 73,227,080 (GRCm39) |
I98S |
probably null |
Het |
Spef2 |
C |
T |
15: 9,653,031 (GRCm39) |
V917M |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,426,399 (GRCm39) |
C139* |
probably null |
Het |
Tenm4 |
A |
G |
7: 96,543,909 (GRCm39) |
D2012G |
probably damaging |
Het |
Tgm5 |
G |
A |
2: 120,883,289 (GRCm39) |
R351C |
probably damaging |
Het |
Tmem145 |
G |
A |
7: 25,006,753 (GRCm39) |
W82* |
probably null |
Het |
Topors |
T |
A |
4: 40,262,654 (GRCm39) |
D210V |
probably damaging |
Het |
Tssk4 |
A |
T |
14: 55,888,569 (GRCm39) |
H146L |
probably damaging |
Het |
Unc93b1 |
T |
A |
19: 3,985,250 (GRCm39) |
D19E |
unknown |
Het |
Usp17lc |
A |
G |
7: 103,067,688 (GRCm39) |
T328A |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,490,252 (GRCm39) |
Y43H |
probably benign |
Het |
Vmn1r25 |
T |
A |
6: 57,955,549 (GRCm39) |
I247F |
probably damaging |
Het |
Vmn2r78 |
A |
T |
7: 86,570,343 (GRCm39) |
Q287L |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,870,371 (GRCm39) |
I3170N |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,236,720 (GRCm39) |
M398K |
probably benign |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp773 |
T |
C |
7: 7,135,907 (GRCm39) |
R230G |
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 |
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 |
|
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 |
|