Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck5 |
A |
T |
15: 76,479,396 (GRCm39) |
I484F |
possibly damaging |
Het |
Ago2 |
A |
T |
15: 73,009,881 (GRCm39) |
N100K |
probably benign |
Het |
Appl1 |
T |
A |
14: 26,681,409 (GRCm39) |
K130* |
probably null |
Het |
Arhgap39 |
G |
A |
15: 76,649,797 (GRCm39) |
|
probably benign |
Het |
Axdnd1 |
A |
G |
1: 156,245,802 (GRCm39) |
|
probably null |
Het |
Camta1 |
A |
T |
4: 151,168,327 (GRCm39) |
V1332E |
probably benign |
Het |
Cd3g |
A |
G |
9: 44,884,857 (GRCm39) |
L129P |
probably damaging |
Het |
Cd80 |
T |
G |
16: 38,294,251 (GRCm39) |
S45A |
probably benign |
Het |
Cdk12 |
A |
T |
11: 98,136,106 (GRCm39) |
Q1120L |
unknown |
Het |
Clip1 |
G |
A |
5: 123,791,696 (GRCm39) |
S158F |
probably benign |
Het |
Cntn3 |
C |
A |
6: 102,255,416 (GRCm39) |
E161* |
probably null |
Het |
Cyp3a59 |
A |
C |
5: 146,024,215 (GRCm39) |
K67T |
probably benign |
Het |
Dmxl1 |
T |
C |
18: 49,997,681 (GRCm39) |
L623P |
probably damaging |
Het |
Drd3 |
T |
A |
16: 43,637,426 (GRCm39) |
Y208* |
probably null |
Het |
Dusp10 |
A |
T |
1: 183,801,153 (GRCm39) |
M307L |
probably benign |
Het |
Dync2li1 |
A |
T |
17: 84,955,141 (GRCm39) |
I267L |
possibly damaging |
Het |
Dynlt2b |
T |
A |
16: 32,244,089 (GRCm39) |
V95E |
probably damaging |
Het |
Edn3 |
C |
A |
2: 174,603,544 (GRCm39) |
C97* |
probably null |
Het |
Ehbp1l1 |
T |
A |
19: 5,769,456 (GRCm39) |
T616S |
possibly damaging |
Het |
Eif2a |
C |
T |
3: 58,452,963 (GRCm39) |
T246I |
probably damaging |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Errfi1 |
A |
G |
4: 150,951,108 (GRCm39) |
T179A |
probably damaging |
Het |
Esyt3 |
G |
A |
9: 99,203,615 (GRCm39) |
L450F |
probably damaging |
Het |
Evx2 |
A |
G |
2: 74,489,448 (GRCm39) |
S106P |
probably benign |
Het |
Fam83a |
T |
G |
15: 57,873,086 (GRCm39) |
V305G |
probably benign |
Het |
Fem1al |
T |
C |
11: 29,774,122 (GRCm39) |
D445G |
probably benign |
Het |
Gpr171 |
T |
A |
3: 59,005,860 (GRCm39) |
|
probably null |
Het |
Grip1 |
A |
G |
10: 119,922,871 (GRCm39) |
T1106A |
probably benign |
Het |
Hecw1 |
A |
G |
13: 14,531,789 (GRCm39) |
Y162H |
probably damaging |
Het |
Hephl1 |
C |
T |
9: 15,009,178 (GRCm39) |
|
probably null |
Het |
Hsp90aa1 |
A |
G |
12: 110,658,562 (GRCm39) |
I693T |
possibly damaging |
Het |
Ifit1bl2 |
T |
A |
19: 34,596,974 (GRCm39) |
D214V |
probably damaging |
Het |
Igsf10 |
T |
C |
3: 59,239,222 (GRCm39) |
M320V |
probably benign |
Het |
Kcnq2 |
A |
G |
2: 180,754,887 (GRCm39) |
L220P |
probably damaging |
Het |
Kpna1 |
C |
A |
16: 35,850,009 (GRCm39) |
Q372K |
probably damaging |
Het |
Lilrb4a |
T |
G |
10: 51,367,149 (GRCm39) |
|
probably null |
Het |
Ly75 |
C |
A |
2: 60,164,818 (GRCm39) |
E787* |
probably null |
Het |
Magi1 |
T |
G |
6: 93,722,562 (GRCm39) |
S666R |
possibly damaging |
Het |
Mif |
C |
A |
10: 75,695,687 (GRCm39) |
A39S |
possibly damaging |
Het |
Mob4 |
G |
A |
1: 55,170,625 (GRCm39) |
|
probably benign |
Het |
Mtmr4 |
G |
T |
11: 87,502,727 (GRCm39) |
C927F |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,110,006 (GRCm39) |
K1398R |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,356,204 (GRCm39) |
Q1137R |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,356,205 (GRCm39) |
Q1137K |
not run |
Het |
Nckap5l |
G |
A |
15: 99,325,357 (GRCm39) |
P382L |
probably damaging |
Het |
Ngly1 |
T |
C |
14: 16,290,844 (GRCm38) |
I442T |
probably damaging |
Het |
Nhsl3 |
C |
A |
4: 129,115,835 (GRCm39) |
R988L |
possibly damaging |
Het |
Nlrp1a |
T |
C |
11: 70,983,237 (GRCm39) |
Y1243C |
probably damaging |
Het |
Or8k53 |
T |
A |
2: 86,177,150 (GRCm39) |
H320L |
possibly damaging |
Het |
Pcsk5 |
C |
T |
19: 17,487,600 (GRCm39) |
G1027D |
probably benign |
Het |
Pla2g2c |
T |
A |
4: 138,458,927 (GRCm39) |
I11N |
probably benign |
Het |
Polr3d |
A |
G |
14: 70,677,240 (GRCm39) |
I331T |
probably damaging |
Het |
Ppp4r4 |
A |
G |
12: 103,551,985 (GRCm39) |
I293M |
possibly damaging |
Het |
Prkce |
G |
T |
17: 86,866,687 (GRCm39) |
V516F |
probably damaging |
Het |
Prss27 |
T |
A |
17: 24,264,683 (GRCm39) |
L282Q |
probably damaging |
Het |
Pxdn |
A |
G |
12: 30,034,926 (GRCm39) |
Y261C |
probably damaging |
Het |
R3hcc1l |
T |
C |
19: 42,551,101 (GRCm39) |
S33P |
probably benign |
Het |
Rab11fip3 |
G |
C |
17: 26,287,848 (GRCm39) |
R102G |
possibly damaging |
Het |
Rabggta |
A |
T |
14: 55,956,773 (GRCm39) |
N310K |
probably null |
Het |
Rbbp8 |
T |
A |
18: 11,793,934 (GRCm39) |
D15E |
probably benign |
Het |
Rbm5 |
T |
C |
9: 107,623,378 (GRCm39) |
Y486C |
probably damaging |
Het |
Rptor |
T |
A |
11: 119,775,805 (GRCm39) |
F992Y |
probably benign |
Het |
Slc29a2 |
T |
G |
19: 5,076,445 (GRCm39) |
L111R |
probably damaging |
Het |
Slc39a11 |
T |
A |
11: 113,452,849 (GRCm39) |
I31L |
probably benign |
Het |
Slc6a20a |
T |
A |
9: 123,485,289 (GRCm39) |
N311I |
possibly damaging |
Het |
Slc8a1 |
A |
G |
17: 81,956,435 (GRCm39) |
F201S |
probably damaging |
Het |
Smtn |
C |
A |
11: 3,480,196 (GRCm39) |
V342L |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,074,853 (GRCm39) |
T4598A |
probably benign |
Het |
Tchp |
A |
G |
5: 114,853,716 (GRCm39) |
T267A |
probably benign |
Het |
Tes3-ps |
A |
G |
13: 49,647,508 (GRCm39) |
E128G |
possibly damaging |
Het |
Tigar |
C |
T |
6: 127,065,129 (GRCm39) |
G173E |
probably benign |
Het |
Tmem171 |
T |
C |
13: 98,824,862 (GRCm39) |
N256S |
probably benign |
Het |
Tmem204 |
A |
G |
17: 25,277,270 (GRCm39) |
I205T |
probably damaging |
Het |
Tmem63a |
A |
G |
1: 180,785,588 (GRCm39) |
K240R |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,019,351 (GRCm39) |
T446M |
probably damaging |
Het |
Tnxb |
A |
T |
17: 34,937,444 (GRCm39) |
N2931I |
probably damaging |
Het |
Trrap |
G |
T |
5: 144,776,284 (GRCm39) |
R2941L |
probably damaging |
Het |
Ttc8 |
A |
T |
12: 98,910,131 (GRCm39) |
R179S |
probably damaging |
Het |
Ttll12 |
G |
T |
15: 83,471,176 (GRCm39) |
T234N |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,577,576 (GRCm39) |
T24439K |
probably damaging |
Het |
Ube2z |
A |
T |
11: 95,946,736 (GRCm39) |
I246N |
possibly damaging |
Het |
Usp15 |
A |
G |
10: 123,011,786 (GRCm39) |
Y104H |
probably damaging |
Het |
Usp29 |
A |
C |
7: 6,964,219 (GRCm39) |
T21P |
possibly damaging |
Het |
Usp5 |
G |
A |
6: 124,798,077 (GRCm39) |
A436V |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,608,354 (GRCm39) |
L1561S |
probably damaging |
Het |
Xrn1 |
A |
G |
9: 95,927,547 (GRCm39) |
M1444V |
probably benign |
Het |
Zfp236 |
G |
T |
18: 82,651,815 (GRCm39) |
Q885K |
probably damaging |
Het |
Zfp831 |
C |
A |
2: 174,487,896 (GRCm39) |
P857Q |
possibly damaging |
Het |
|
Other mutations in Myo3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01014:Myo3a
|
APN |
2 |
22,337,284 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01307:Myo3a
|
APN |
2 |
22,448,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01413:Myo3a
|
APN |
2 |
22,302,411 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01655:Myo3a
|
APN |
2 |
22,428,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01767:Myo3a
|
APN |
2 |
22,428,033 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01803:Myo3a
|
APN |
2 |
22,245,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01969:Myo3a
|
APN |
2 |
22,302,499 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02043:Myo3a
|
APN |
2 |
22,404,776 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02124:Myo3a
|
APN |
2 |
22,467,538 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02174:Myo3a
|
APN |
2 |
22,337,204 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02649:Myo3a
|
APN |
2 |
22,328,418 (GRCm39) |
missense |
probably benign |
|
IGL02976:Myo3a
|
APN |
2 |
22,434,494 (GRCm39) |
nonsense |
probably null |
|
IGL03328:Myo3a
|
APN |
2 |
22,468,210 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03376:Myo3a
|
APN |
2 |
22,490,086 (GRCm39) |
splice site |
probably benign |
|
lose
|
UTSW |
2 |
22,448,332 (GRCm39) |
nonsense |
probably null |
|
snooze
|
UTSW |
2 |
22,287,445 (GRCm39) |
missense |
probably damaging |
0.99 |
A5278:Myo3a
|
UTSW |
2 |
22,328,464 (GRCm39) |
missense |
probably benign |
0.27 |
PIT4445001:Myo3a
|
UTSW |
2 |
22,434,457 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0008:Myo3a
|
UTSW |
2 |
22,469,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R0099:Myo3a
|
UTSW |
2 |
22,250,409 (GRCm39) |
missense |
probably benign |
0.03 |
R0103:Myo3a
|
UTSW |
2 |
22,436,360 (GRCm39) |
splice site |
probably benign |
|
R0103:Myo3a
|
UTSW |
2 |
22,436,360 (GRCm39) |
splice site |
probably benign |
|
R0212:Myo3a
|
UTSW |
2 |
22,296,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Myo3a
|
UTSW |
2 |
22,250,409 (GRCm39) |
missense |
probably benign |
0.03 |
R0282:Myo3a
|
UTSW |
2 |
22,250,409 (GRCm39) |
missense |
probably benign |
0.03 |
R0492:Myo3a
|
UTSW |
2 |
22,328,447 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0498:Myo3a
|
UTSW |
2 |
22,467,441 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0594:Myo3a
|
UTSW |
2 |
22,436,370 (GRCm39) |
splice site |
probably benign |
|
R0609:Myo3a
|
UTSW |
2 |
22,401,110 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0609:Myo3a
|
UTSW |
2 |
22,338,324 (GRCm39) |
missense |
probably benign |
0.29 |
R0827:Myo3a
|
UTSW |
2 |
22,448,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R0968:Myo3a
|
UTSW |
2 |
22,448,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R1157:Myo3a
|
UTSW |
2 |
22,434,456 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1301:Myo3a
|
UTSW |
2 |
22,271,906 (GRCm39) |
splice site |
probably benign |
|
R1352:Myo3a
|
UTSW |
2 |
22,328,486 (GRCm39) |
critical splice donor site |
probably null |
|
R1443:Myo3a
|
UTSW |
2 |
22,287,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Myo3a
|
UTSW |
2 |
22,467,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1465:Myo3a
|
UTSW |
2 |
22,467,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1517:Myo3a
|
UTSW |
2 |
22,287,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R1565:Myo3a
|
UTSW |
2 |
22,345,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Myo3a
|
UTSW |
2 |
22,455,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Myo3a
|
UTSW |
2 |
22,404,638 (GRCm39) |
missense |
probably benign |
0.03 |
R1822:Myo3a
|
UTSW |
2 |
22,345,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Myo3a
|
UTSW |
2 |
22,345,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Myo3a
|
UTSW |
2 |
22,401,054 (GRCm39) |
missense |
probably benign |
|
R1837:Myo3a
|
UTSW |
2 |
22,467,604 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1867:Myo3a
|
UTSW |
2 |
22,404,657 (GRCm39) |
missense |
probably benign |
0.00 |
R1917:Myo3a
|
UTSW |
2 |
22,296,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Myo3a
|
UTSW |
2 |
22,455,008 (GRCm39) |
missense |
probably benign |
0.02 |
R1937:Myo3a
|
UTSW |
2 |
22,401,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Myo3a
|
UTSW |
2 |
22,246,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Myo3a
|
UTSW |
2 |
22,468,140 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2091:Myo3a
|
UTSW |
2 |
22,338,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R2115:Myo3a
|
UTSW |
2 |
22,250,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Myo3a
|
UTSW |
2 |
22,468,186 (GRCm39) |
missense |
probably benign |
0.42 |
R2126:Myo3a
|
UTSW |
2 |
22,468,186 (GRCm39) |
missense |
probably benign |
0.42 |
R2216:Myo3a
|
UTSW |
2 |
22,467,783 (GRCm39) |
missense |
probably benign |
0.00 |
R2413:Myo3a
|
UTSW |
2 |
22,467,924 (GRCm39) |
missense |
probably benign |
0.00 |
R2964:Myo3a
|
UTSW |
2 |
22,345,067 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3196:Myo3a
|
UTSW |
2 |
22,404,679 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3837:Myo3a
|
UTSW |
2 |
22,455,121 (GRCm39) |
splice site |
probably benign |
|
R3905:Myo3a
|
UTSW |
2 |
22,448,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Myo3a
|
UTSW |
2 |
22,455,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R4014:Myo3a
|
UTSW |
2 |
22,468,182 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4015:Myo3a
|
UTSW |
2 |
22,468,182 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4017:Myo3a
|
UTSW |
2 |
22,468,182 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4043:Myo3a
|
UTSW |
2 |
22,338,350 (GRCm39) |
splice site |
probably benign |
|
R4044:Myo3a
|
UTSW |
2 |
22,467,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R4057:Myo3a
|
UTSW |
2 |
22,270,971 (GRCm39) |
missense |
probably benign |
0.01 |
R4192:Myo3a
|
UTSW |
2 |
22,412,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Myo3a
|
UTSW |
2 |
22,345,089 (GRCm39) |
missense |
probably benign |
0.14 |
R4321:Myo3a
|
UTSW |
2 |
22,271,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Myo3a
|
UTSW |
2 |
22,467,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R4398:Myo3a
|
UTSW |
2 |
22,467,854 (GRCm39) |
missense |
probably benign |
|
R4446:Myo3a
|
UTSW |
2 |
22,490,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4685:Myo3a
|
UTSW |
2 |
22,412,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Myo3a
|
UTSW |
2 |
22,287,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5096:Myo3a
|
UTSW |
2 |
22,464,254 (GRCm39) |
missense |
probably benign |
0.16 |
R5183:Myo3a
|
UTSW |
2 |
22,468,170 (GRCm39) |
missense |
probably benign |
0.05 |
R5458:Myo3a
|
UTSW |
2 |
22,250,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Myo3a
|
UTSW |
2 |
22,448,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R5522:Myo3a
|
UTSW |
2 |
22,464,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Myo3a
|
UTSW |
2 |
22,448,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R6479:Myo3a
|
UTSW |
2 |
22,467,877 (GRCm39) |
missense |
probably benign |
0.00 |
R6513:Myo3a
|
UTSW |
2 |
22,412,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Myo3a
|
UTSW |
2 |
22,404,737 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6602:Myo3a
|
UTSW |
2 |
22,467,799 (GRCm39) |
missense |
probably damaging |
0.96 |
R6671:Myo3a
|
UTSW |
2 |
22,299,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R6743:Myo3a
|
UTSW |
2 |
22,366,475 (GRCm39) |
missense |
probably benign |
0.24 |
R6865:Myo3a
|
UTSW |
2 |
22,464,313 (GRCm39) |
missense |
probably benign |
0.00 |
R6961:Myo3a
|
UTSW |
2 |
22,250,369 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Myo3a
|
UTSW |
2 |
22,337,188 (GRCm39) |
missense |
probably benign |
0.04 |
R7215:Myo3a
|
UTSW |
2 |
22,250,378 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7301:Myo3a
|
UTSW |
2 |
22,436,504 (GRCm39) |
critical splice donor site |
probably null |
|
R7318:Myo3a
|
UTSW |
2 |
22,448,332 (GRCm39) |
nonsense |
probably null |
|
R7456:Myo3a
|
UTSW |
2 |
22,412,255 (GRCm39) |
missense |
probably benign |
0.08 |
R7528:Myo3a
|
UTSW |
2 |
22,270,925 (GRCm39) |
nonsense |
probably null |
|
R7731:Myo3a
|
UTSW |
2 |
22,287,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Myo3a
|
UTSW |
2 |
22,245,954 (GRCm39) |
missense |
probably damaging |
0.99 |
R8054:Myo3a
|
UTSW |
2 |
22,464,329 (GRCm39) |
missense |
probably benign |
0.00 |
R8140:Myo3a
|
UTSW |
2 |
22,412,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Myo3a
|
UTSW |
2 |
22,287,476 (GRCm39) |
critical splice donor site |
probably null |
|
R8346:Myo3a
|
UTSW |
2 |
22,448,434 (GRCm39) |
critical splice donor site |
probably null |
|
R8421:Myo3a
|
UTSW |
2 |
22,366,935 (GRCm39) |
missense |
probably benign |
0.07 |
R8495:Myo3a
|
UTSW |
2 |
22,401,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R8551:Myo3a
|
UTSW |
2 |
22,337,277 (GRCm39) |
missense |
probably benign |
0.00 |
R8708:Myo3a
|
UTSW |
2 |
22,296,607 (GRCm39) |
splice site |
probably benign |
|
R8757:Myo3a
|
UTSW |
2 |
22,448,319 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8759:Myo3a
|
UTSW |
2 |
22,448,319 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8779:Myo3a
|
UTSW |
2 |
22,250,404 (GRCm39) |
nonsense |
probably null |
|
R8828:Myo3a
|
UTSW |
2 |
22,245,864 (GRCm39) |
missense |
probably benign |
0.01 |
R8910:Myo3a
|
UTSW |
2 |
22,464,280 (GRCm39) |
missense |
probably benign |
0.01 |
R8916:Myo3a
|
UTSW |
2 |
22,457,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Myo3a
|
UTSW |
2 |
22,401,074 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9028:Myo3a
|
UTSW |
2 |
22,490,099 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9046:Myo3a
|
UTSW |
2 |
22,448,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R9120:Myo3a
|
UTSW |
2 |
22,436,464 (GRCm39) |
missense |
probably benign |
0.27 |
R9153:Myo3a
|
UTSW |
2 |
22,404,744 (GRCm39) |
missense |
probably benign |
0.02 |
R9191:Myo3a
|
UTSW |
2 |
22,469,841 (GRCm39) |
missense |
probably benign |
0.24 |
R9258:Myo3a
|
UTSW |
2 |
22,467,545 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9436:Myo3a
|
UTSW |
2 |
22,412,235 (GRCm39) |
nonsense |
probably null |
|
R9464:Myo3a
|
UTSW |
2 |
22,232,383 (GRCm39) |
start gained |
probably benign |
|
R9487:Myo3a
|
UTSW |
2 |
22,245,862 (GRCm39) |
missense |
probably benign |
|
R9719:Myo3a
|
UTSW |
2 |
22,436,493 (GRCm39) |
missense |
probably benign |
0.02 |
R9799:Myo3a
|
UTSW |
2 |
22,490,181 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo3a
|
UTSW |
2 |
22,508,152 (GRCm39) |
missense |
possibly damaging |
0.58 |
|