Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
A |
T |
16: 56,507,455 (GRCm39) |
Y1091F |
probably damaging |
Het |
Arl8b |
A |
G |
6: 108,792,250 (GRCm39) |
I104V |
probably benign |
Het |
Asb2 |
C |
A |
12: 103,304,457 (GRCm39) |
G16C |
probably benign |
Het |
Bptf |
T |
C |
11: 106,945,836 (GRCm39) |
S2468G |
probably damaging |
Het |
Capns1 |
T |
A |
7: 29,889,963 (GRCm39) |
D182V |
probably damaging |
Het |
Cct5 |
T |
C |
15: 31,594,658 (GRCm39) |
H182R |
possibly damaging |
Het |
Cd200 |
G |
A |
16: 45,215,157 (GRCm39) |
R165C |
probably benign |
Het |
Chd3 |
C |
T |
11: 69,247,097 (GRCm39) |
V1024I |
probably damaging |
Het |
Chd8 |
CAGGGTCTGCCCTCATGGTATTGTATTTCTCATAGCCTAAAAGAACAAGGG |
C |
14: 52,448,037 (GRCm39) |
|
probably null |
Het |
Csmd1 |
T |
C |
8: 16,048,794 (GRCm39) |
S2303G |
probably benign |
Het |
Ctsl |
A |
G |
13: 64,514,314 (GRCm39) |
S255P |
probably damaging |
Het |
Dclre1c |
T |
G |
2: 3,444,714 (GRCm39) |
N268K |
possibly damaging |
Het |
Dock10 |
T |
C |
1: 80,521,134 (GRCm39) |
D1158G |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,757,797 (GRCm39) |
D102E |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,344,495 (GRCm39) |
D290E |
probably damaging |
Het |
Fam72a |
T |
A |
1: 131,458,461 (GRCm39) |
C74* |
probably null |
Het |
Gnrh1 |
T |
A |
14: 67,985,334 (GRCm39) |
L73Q |
probably damaging |
Het |
Grina |
T |
A |
15: 76,132,497 (GRCm39) |
S115T |
probably damaging |
Het |
Grm3 |
A |
T |
5: 9,554,725 (GRCm39) |
S856T |
probably benign |
Het |
Hars1 |
C |
A |
18: 36,899,996 (GRCm39) |
R490L |
possibly damaging |
Het |
Ide |
T |
A |
19: 37,292,241 (GRCm39) |
K318I |
|
Het |
Immt |
C |
A |
6: 71,829,762 (GRCm39) |
S156* |
probably null |
Het |
Iqcd |
A |
G |
5: 120,738,232 (GRCm39) |
I17V |
possibly damaging |
Het |
Klhdc1 |
T |
C |
12: 69,298,808 (GRCm39) |
V131A |
probably damaging |
Het |
Klk6 |
C |
A |
7: 43,478,061 (GRCm39) |
N144K |
|
Het |
Klk6 |
T |
C |
7: 43,478,062 (GRCm39) |
C145R |
probably damaging |
Het |
Lrfn2 |
A |
T |
17: 49,404,132 (GRCm39) |
T752S |
probably damaging |
Het |
Lrguk |
A |
C |
6: 34,080,572 (GRCm39) |
Q1269P |
unknown |
Het |
Lrwd1 |
G |
T |
5: 136,164,787 (GRCm39) |
Q7K |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,302,204 (GRCm39) |
M766K |
probably benign |
Het |
Neb |
T |
C |
2: 52,084,438 (GRCm39) |
Y5587C |
probably damaging |
Het |
Nf1 |
A |
T |
11: 79,286,679 (GRCm39) |
|
probably null |
Het |
Npepps |
G |
T |
11: 97,131,823 (GRCm39) |
R344S |
probably damaging |
Het |
Nudt16l2 |
C |
T |
9: 105,021,648 (GRCm39) |
D133N |
probably damaging |
Het |
Or52p1 |
A |
T |
7: 104,267,486 (GRCm39) |
Y200F |
probably damaging |
Het |
Or5v1b |
A |
G |
17: 37,841,333 (GRCm39) |
N155S |
probably damaging |
Het |
Pcnx1 |
T |
A |
12: 82,042,597 (GRCm39) |
W2286R |
probably damaging |
Het |
Ppm1g |
A |
T |
5: 31,365,768 (GRCm39) |
N51K |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,799,981 (GRCm39) |
K722E |
probably damaging |
Het |
Prim1 |
A |
G |
10: 127,859,761 (GRCm39) |
S318G |
probably damaging |
Het |
Prl4a1 |
T |
C |
13: 28,207,307 (GRCm39) |
Y194H |
probably damaging |
Het |
Prl7c1 |
A |
T |
13: 27,957,854 (GRCm39) |
D195E |
probably benign |
Het |
Psmb2 |
A |
G |
4: 126,603,330 (GRCm39) |
D186G |
probably benign |
Het |
Ptprq |
A |
G |
10: 107,482,513 (GRCm39) |
V1020A |
probably benign |
Het |
Scgb2b20 |
T |
C |
7: 33,065,689 (GRCm39) |
T13A |
unknown |
Het |
Scly |
C |
A |
1: 91,244,830 (GRCm39) |
H310Q |
possibly damaging |
Het |
Sdccag8 |
G |
A |
1: 176,783,473 (GRCm39) |
E661K |
probably damaging |
Het |
Sema4f |
G |
A |
6: 82,894,873 (GRCm39) |
L441F |
probably benign |
Het |
Sema4f |
A |
C |
6: 82,894,874 (GRCm39) |
Y440* |
probably null |
Het |
Tmem262 |
C |
T |
19: 6,130,118 (GRCm39) |
|
probably benign |
Het |
Trim33 |
A |
G |
3: 103,236,392 (GRCm39) |
T501A |
probably damaging |
Het |
Trio |
C |
A |
15: 27,741,150 (GRCm39) |
V2692F |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,772,774 (GRCm39) |
V2453E |
unknown |
Het |
Ttn |
G |
T |
2: 76,541,956 (GRCm39) |
R33677S |
probably benign |
Het |
Uaca |
T |
A |
9: 60,778,852 (GRCm39) |
S1080T |
probably benign |
Het |
Vav3 |
T |
A |
3: 109,555,051 (GRCm39) |
C660S |
probably benign |
Het |
Vmn1r229 |
T |
A |
17: 21,034,990 (GRCm39) |
D78E |
probably damaging |
Het |
Vmn2r73 |
A |
G |
7: 85,521,179 (GRCm39) |
V263A |
probably damaging |
Het |
Yeats2 |
A |
T |
16: 19,969,260 (GRCm39) |
D17V |
probably benign |
Het |
Zfp658 |
T |
A |
7: 43,222,240 (GRCm39) |
W172R |
probably benign |
Het |
Zfp804a |
A |
C |
2: 82,089,459 (GRCm39) |
H1096P |
possibly damaging |
Het |
Zkscan14 |
C |
T |
5: 145,138,375 (GRCm39) |
W37* |
probably null |
Het |
Zmynd15 |
A |
T |
11: 70,355,017 (GRCm39) |
D468V |
probably damaging |
Het |
Zmynd8 |
A |
T |
2: 165,654,466 (GRCm39) |
V682E |
probably benign |
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 |
|
R7447:Myo3a
|
UTSW |
2 |
22,436,464 (GRCm39) |
missense |
probably benign |
0.27 |
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 |
|
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 |
|