Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
T |
A |
1: 173,159,598 (GRCm39) |
H307L |
probably benign |
Het |
Acnat1 |
A |
T |
4: 49,450,652 (GRCm39) |
L153H |
probably damaging |
Het |
Actn4 |
A |
T |
7: 28,618,431 (GRCm39) |
D76E |
probably benign |
Het |
Afdn |
A |
C |
17: 14,066,782 (GRCm39) |
M640L |
probably benign |
Het |
Angpt1 |
A |
T |
15: 42,539,837 (GRCm39) |
F7L |
probably benign |
Het |
Ap3b2 |
A |
G |
7: 81,126,092 (GRCm39) |
F373S |
probably damaging |
Het |
Armc2 |
T |
A |
10: 41,800,457 (GRCm39) |
Y650F |
probably damaging |
Het |
Atg2b |
G |
T |
12: 105,630,197 (GRCm39) |
T398K |
possibly damaging |
Het |
Baz1a |
CCATT |
CCATTCATT |
12: 55,021,895 (GRCm39) |
|
probably null |
Het |
Capn8 |
G |
A |
1: 182,438,670 (GRCm39) |
|
probably null |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,637,081 (GRCm39) |
N3103D |
probably benign |
Het |
Chd9 |
G |
A |
8: 91,738,063 (GRCm39) |
R1565Q |
unknown |
Het |
Cir1 |
G |
A |
2: 73,134,152 (GRCm39) |
T139I |
probably damaging |
Het |
Cmah |
T |
C |
13: 24,619,673 (GRCm39) |
|
probably null |
Het |
Cnpy1 |
T |
C |
5: 28,450,800 (GRCm39) |
D2G |
probably damaging |
Het |
Dennd4a |
A |
T |
9: 64,801,793 (GRCm39) |
T979S |
probably benign |
Het |
Dnah11 |
T |
A |
12: 117,842,311 (GRCm39) |
K4423* |
probably null |
Het |
Dnajb4 |
A |
G |
3: 151,892,320 (GRCm39) |
I171T |
possibly damaging |
Het |
Dpm1 |
A |
T |
2: 168,072,307 (GRCm39) |
|
probably null |
Het |
Dtwd1 |
A |
G |
2: 125,996,595 (GRCm39) |
T27A |
probably benign |
Het |
Ep400 |
C |
T |
5: 110,889,872 (GRCm39) |
D464N |
unknown |
Het |
Epb42 |
A |
T |
2: 120,855,091 (GRCm39) |
I498N |
probably benign |
Het |
Fhod1 |
A |
G |
8: 106,064,048 (GRCm39) |
V219A |
unknown |
Het |
Gabrb2 |
A |
T |
11: 42,517,436 (GRCm39) |
E419D |
probably benign |
Het |
Galnt18 |
A |
T |
7: 111,071,168 (GRCm39) |
N615K |
possibly damaging |
Het |
Gm29106 |
T |
A |
1: 118,127,254 (GRCm39) |
H315Q |
possibly damaging |
Het |
Gprin2 |
G |
T |
14: 33,917,615 (GRCm39) |
Q52K |
probably benign |
Het |
Grm4 |
A |
T |
17: 27,657,765 (GRCm39) |
Y414N |
probably damaging |
Het |
Gulo |
C |
A |
14: 66,225,630 (GRCm39) |
|
probably null |
Het |
H2-M1 |
A |
C |
17: 36,980,997 (GRCm39) |
V313G |
possibly damaging |
Het |
Hectd3 |
T |
C |
4: 116,852,951 (GRCm39) |
W118R |
probably damaging |
Het |
Hs6st3 |
G |
A |
14: 120,106,492 (GRCm39) |
C300Y |
probably damaging |
Het |
Il1rl2 |
T |
A |
1: 40,404,519 (GRCm39) |
S547T |
possibly damaging |
Het |
Kank1 |
G |
T |
19: 25,386,872 (GRCm39) |
V182F |
probably damaging |
Het |
Kif20b |
T |
A |
19: 34,928,149 (GRCm39) |
L1137* |
probably null |
Het |
Klhl7 |
A |
G |
5: 24,331,818 (GRCm39) |
|
probably null |
Het |
Krt13 |
T |
A |
11: 100,011,987 (GRCm39) |
D112V |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,290,064 (GRCm39) |
V71A |
probably benign |
Het |
Ly6g |
T |
C |
15: 75,030,458 (GRCm39) |
V92A |
probably benign |
Het |
Map2k3 |
G |
A |
11: 60,822,929 (GRCm39) |
|
probably benign |
Het |
Mast2 |
A |
C |
4: 116,168,927 (GRCm39) |
D842E |
probably benign |
Het |
Mpo |
T |
G |
11: 87,694,349 (GRCm39) |
M693R |
probably benign |
Het |
Nadk2 |
C |
T |
15: 9,106,824 (GRCm39) |
R37* |
probably null |
Het |
Ncapd3 |
G |
A |
9: 26,974,655 (GRCm39) |
R709H |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,572,892 (GRCm39) |
Y55* |
probably null |
Het |
Neurl4 |
A |
G |
11: 69,798,301 (GRCm39) |
D777G |
probably damaging |
Het |
Npr2 |
G |
A |
4: 43,633,527 (GRCm39) |
V224M |
possibly damaging |
Het |
Nptx2 |
T |
A |
5: 144,484,950 (GRCm39) |
S148T |
probably benign |
Het |
Nr1d1 |
T |
C |
11: 98,661,160 (GRCm39) |
T369A |
probably benign |
Het |
Nub1 |
T |
G |
5: 24,908,483 (GRCm39) |
F411V |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,194,300 (GRCm39) |
Y158N |
probably damaging |
Het |
Or2d36 |
A |
T |
7: 106,746,660 (GRCm39) |
I46F |
probably benign |
Het |
Or5e1 |
A |
G |
7: 108,354,639 (GRCm39) |
N192S |
probably benign |
Het |
Or5m8 |
A |
G |
2: 85,823,091 (GRCm39) |
Y310C |
probably benign |
Het |
Or6c6c |
A |
T |
10: 129,541,208 (GRCm39) |
I154F |
probably damaging |
Het |
Or8c19-ps1 |
T |
A |
9: 38,220,928 (GRCm39) |
I279K |
unknown |
Het |
Orc2 |
C |
T |
1: 58,536,610 (GRCm39) |
G85S |
probably damaging |
Het |
Pak1ip1 |
T |
A |
13: 41,162,743 (GRCm39) |
V182D |
probably damaging |
Het |
Parvg |
T |
G |
15: 84,210,424 (GRCm39) |
C30W |
probably benign |
Het |
Pcdha1 |
T |
A |
18: 37,065,713 (GRCm39) |
D792E |
probably benign |
Het |
Ppp1r13b |
G |
T |
12: 111,800,242 (GRCm39) |
Q635K |
probably benign |
Het |
Pramel26 |
T |
C |
4: 143,536,886 (GRCm39) |
T482A |
probably benign |
Het |
Psg16 |
A |
G |
7: 16,832,086 (GRCm39) |
I341V |
probably benign |
Het |
Psme4 |
C |
T |
11: 30,826,868 (GRCm39) |
Q1796* |
probably null |
Het |
Ptn |
T |
G |
6: 36,692,699 (GRCm39) |
|
probably null |
Het |
Rapsn |
C |
T |
2: 90,875,823 (GRCm39) |
P400L |
probably damaging |
Het |
Rasal1 |
G |
A |
5: 120,800,358 (GRCm39) |
G207D |
probably damaging |
Het |
Rdx |
A |
G |
9: 51,974,878 (GRCm39) |
I5V |
probably benign |
Het |
Rpf1 |
A |
G |
3: 146,223,533 (GRCm39) |
I105T |
probably damaging |
Het |
Rps15a |
A |
T |
7: 117,709,220 (GRCm39) |
F79I |
possibly damaging |
Het |
Rwdd2b |
G |
A |
16: 87,233,641 (GRCm39) |
P153L |
probably benign |
Het |
Scaf11 |
G |
A |
15: 96,318,298 (GRCm39) |
S422L |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,403 (GRCm39) |
E287V |
possibly damaging |
Het |
Sgta |
T |
C |
10: 80,887,118 (GRCm39) |
D49G |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,025,358 (GRCm39) |
M1068K |
probably benign |
Het |
Slc12a9 |
G |
A |
5: 137,319,671 (GRCm39) |
R615W |
probably damaging |
Het |
Slc26a3 |
T |
A |
12: 31,499,145 (GRCm39) |
S151T |
probably benign |
Het |
Slc4a8 |
C |
A |
15: 100,681,721 (GRCm39) |
H111N |
probably damaging |
Het |
Syngr1 |
G |
A |
15: 79,975,659 (GRCm39) |
R22K |
probably benign |
Het |
Tars2 |
A |
T |
3: 95,662,077 (GRCm39) |
V25E |
probably benign |
Het |
Tbx15 |
A |
G |
3: 99,259,647 (GRCm39) |
Y506C |
probably damaging |
Het |
Tgm4 |
A |
T |
9: 122,875,634 (GRCm39) |
K162N |
possibly damaging |
Het |
Tmem253 |
A |
G |
14: 52,255,439 (GRCm39) |
E83G |
probably damaging |
Het |
Trp73 |
G |
A |
4: 154,165,859 (GRCm39) |
T118I |
probably damaging |
Het |
Trpm7 |
A |
G |
2: 126,664,578 (GRCm39) |
S934P |
possibly damaging |
Het |
Ttc23l |
G |
A |
15: 10,523,729 (GRCm39) |
S330L |
probably benign |
Het |
Tub |
A |
C |
7: 108,624,845 (GRCm39) |
D199A |
probably benign |
Het |
Uri1 |
A |
C |
7: 37,696,110 (GRCm39) |
|
probably null |
Het |
Usp16 |
C |
T |
16: 87,276,120 (GRCm39) |
A486V |
probably benign |
Het |
Vmn1r12 |
A |
G |
6: 57,136,526 (GRCm39) |
I208V |
probably benign |
Het |
Vmn2r116 |
A |
T |
17: 23,620,797 (GRCm39) |
M844L |
probably benign |
Het |
Vmn2r13 |
C |
T |
5: 109,339,773 (GRCm39) |
|
probably null |
Het |
Xpnpep1 |
T |
C |
19: 53,001,892 (GRCm39) |
D118G |
probably damaging |
Het |
Zfp111 |
G |
A |
7: 23,898,067 (GRCm39) |
P516S |
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 |
|
|
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 |
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 |
|