Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
A |
T |
15: 57,892,132 (GRCm39) |
N158K |
probably benign |
Het |
Acnat1 |
G |
C |
4: 49,447,457 (GRCm39) |
P357A |
probably damaging |
Het |
Akap6 |
T |
A |
12: 53,119,240 (GRCm39) |
C1102* |
probably null |
Het |
Amelx |
T |
C |
X: 167,964,826 (GRCm39) |
|
probably benign |
Het |
Brap |
G |
A |
5: 121,803,259 (GRCm39) |
V136I |
possibly damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Csgalnact1 |
TGG |
TG |
8: 68,913,737 (GRCm39) |
|
probably null |
Het |
Csk |
A |
T |
9: 57,537,556 (GRCm39) |
C119* |
probably null |
Het |
Dcbld1 |
T |
C |
10: 52,195,587 (GRCm39) |
L265P |
probably damaging |
Het |
Desi1 |
T |
A |
15: 81,887,976 (GRCm39) |
K31N |
probably damaging |
Het |
Dpy19l2 |
C |
A |
9: 24,607,285 (GRCm39) |
G59C |
probably damaging |
Het |
Eif2b5 |
T |
C |
16: 20,324,272 (GRCm39) |
V498A |
probably benign |
Het |
Epdr1 |
A |
T |
13: 19,778,815 (GRCm39) |
Y94N |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,404,905 (GRCm39) |
V552A |
probably benign |
Het |
Focad |
A |
G |
4: 88,325,588 (GRCm39) |
E151G |
possibly damaging |
Het |
Frem1 |
A |
G |
4: 82,932,351 (GRCm39) |
F117L |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,444,752 (GRCm39) |
Y2460N |
probably damaging |
Het |
Gm3604 |
A |
T |
13: 62,517,868 (GRCm39) |
C163* |
probably null |
Het |
Gpalpp1 |
A |
C |
14: 76,336,063 (GRCm39) |
|
probably null |
Het |
Grid2ip |
A |
G |
5: 143,373,933 (GRCm39) |
I858V |
probably damaging |
Het |
Grin2b |
ATTGTTGT |
ATTGT |
6: 135,709,453 (GRCm39) |
|
probably benign |
Het |
Hps4 |
A |
G |
5: 112,512,429 (GRCm39) |
T182A |
probably damaging |
Het |
Impa1 |
A |
T |
3: 10,394,075 (GRCm39) |
|
probably null |
Het |
Kcnh3 |
T |
C |
15: 99,131,862 (GRCm39) |
S606P |
probably damaging |
Het |
Kif23 |
T |
A |
9: 61,839,193 (GRCm39) |
R301* |
probably null |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lcp2 |
G |
T |
11: 34,040,670 (GRCm39) |
A529S |
probably benign |
Het |
Lhx8 |
G |
A |
3: 154,035,925 (GRCm39) |
A22V |
probably benign |
Het |
Lin28a |
A |
T |
4: 133,735,235 (GRCm39) |
S134T |
possibly damaging |
Het |
Med27 |
T |
A |
2: 29,236,882 (GRCm39) |
V9E |
possibly damaging |
Het |
Mmp7 |
C |
A |
9: 7,692,219 (GRCm39) |
S31R |
probably benign |
Het |
Mtcl1 |
T |
G |
17: 66,650,829 (GRCm39) |
E1545D |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,409,126 (GRCm39) |
Y187H |
probably damaging |
Het |
Nsmce1 |
T |
C |
7: 125,085,645 (GRCm39) |
M15V |
probably benign |
Het |
Nxpe3 |
A |
T |
16: 55,670,078 (GRCm39) |
N342K |
probably damaging |
Het |
Or7g25 |
A |
G |
9: 19,160,495 (GRCm39) |
S67P |
probably damaging |
Het |
Or8g2 |
T |
A |
9: 39,821,756 (GRCm39) |
I219N |
probably damaging |
Het |
Pcdhb9 |
A |
G |
18: 37,534,663 (GRCm39) |
N219S |
probably benign |
Het |
Pck2 |
T |
A |
14: 55,781,449 (GRCm39) |
V190E |
probably damaging |
Het |
Pde4b |
G |
A |
4: 102,456,840 (GRCm39) |
A429T |
probably damaging |
Het |
Phf1 |
T |
C |
17: 27,153,429 (GRCm39) |
V54A |
probably damaging |
Het |
Pla2r1 |
T |
C |
2: 60,353,127 (GRCm39) |
E278G |
probably damaging |
Het |
Ptges3 |
G |
T |
10: 127,908,016 (GRCm39) |
R122L |
probably benign |
Het |
Rnpepl1 |
C |
T |
1: 92,844,881 (GRCm39) |
T391I |
probably damaging |
Het |
Rps6kb1 |
G |
A |
11: 86,397,633 (GRCm39) |
A404V |
probably benign |
Het |
Rrm2b |
T |
C |
15: 37,945,391 (GRCm39) |
|
probably null |
Het |
Sh3rf1 |
C |
T |
8: 61,679,321 (GRCm39) |
P121L |
probably benign |
Het |
Skint9 |
T |
G |
4: 112,248,148 (GRCm39) |
I199L |
probably benign |
Het |
Slc9b2 |
G |
T |
3: 135,042,290 (GRCm39) |
R523L |
probably benign |
Het |
Slco1c1 |
T |
A |
6: 141,477,174 (GRCm39) |
|
probably null |
Het |
Stox2 |
T |
C |
8: 47,645,865 (GRCm39) |
T532A |
probably damaging |
Het |
Tbcel |
A |
G |
9: 42,327,248 (GRCm39) |
L385P |
probably damaging |
Het |
Tle5 |
A |
G |
10: 81,401,474 (GRCm39) |
N181D |
probably benign |
Het |
Tmem268 |
G |
A |
4: 63,496,149 (GRCm39) |
|
probably null |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Top3a |
G |
A |
11: 60,650,182 (GRCm39) |
T122M |
probably damaging |
Het |
Trav7n-4 |
G |
A |
14: 53,329,088 (GRCm39) |
V33I |
probably benign |
Het |
Ttn |
T |
G |
2: 76,539,551 (GRCm39) |
E26151D |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,687,228 (GRCm39) |
|
probably benign |
Het |
Tyk2 |
A |
G |
9: 21,035,328 (GRCm39) |
C195R |
possibly damaging |
Het |
Ugt2b38 |
T |
C |
5: 87,558,078 (GRCm39) |
K528E |
probably damaging |
Het |
Usp28 |
T |
A |
9: 48,937,125 (GRCm39) |
D483E |
probably benign |
Het |
Vldlr |
A |
G |
19: 27,220,554 (GRCm39) |
D598G |
probably damaging |
Het |
Vmn1r51 |
T |
G |
6: 90,106,498 (GRCm39) |
I138S |
probably damaging |
Het |
Vps13b |
G |
A |
15: 35,869,541 (GRCm39) |
A2682T |
probably damaging |
Het |
Wac |
T |
A |
18: 7,917,568 (GRCm39) |
V346E |
probably damaging |
Het |
Zdbf2 |
T |
C |
1: 63,347,579 (GRCm39) |
V1986A |
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 |
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 |
|
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 |
|