Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
A |
G |
11: 7,080,348 (GRCm39) |
T364A |
probably benign |
Het |
Adpgk |
G |
A |
9: 59,221,036 (GRCm39) |
V281I |
probably benign |
Het |
Akap9 |
C |
A |
5: 4,026,235 (GRCm39) |
Q1297K |
possibly damaging |
Het |
Ankrd13d |
T |
C |
19: 4,331,968 (GRCm39) |
E110G |
probably damaging |
Het |
Ankrd53 |
A |
G |
6: 83,740,244 (GRCm39) |
E104G |
possibly damaging |
Het |
Ano6 |
A |
T |
15: 95,863,855 (GRCm39) |
T792S |
probably benign |
Het |
Atm |
A |
T |
9: 53,421,566 (GRCm39) |
V715D |
probably damaging |
Het |
Avl9 |
A |
G |
6: 56,713,828 (GRCm39) |
D362G |
probably benign |
Het |
Bin1 |
T |
A |
18: 32,547,280 (GRCm39) |
S152R |
probably damaging |
Het |
Bscl2 |
T |
A |
19: 8,818,514 (GRCm39) |
C40S |
probably benign |
Het |
Btaf1 |
A |
G |
19: 36,958,486 (GRCm39) |
T668A |
probably benign |
Het |
Btrc |
A |
G |
19: 45,504,497 (GRCm39) |
D397G |
probably damaging |
Het |
Cables2 |
A |
T |
2: 179,902,222 (GRCm39) |
V379E |
probably damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,389,221 (GRCm39) |
L228P |
probably damaging |
Het |
Cd109 |
A |
T |
9: 78,574,639 (GRCm39) |
D541V |
probably damaging |
Het |
Cdh26 |
A |
T |
2: 178,108,382 (GRCm39) |
S327C |
probably damaging |
Het |
Cep78 |
T |
C |
19: 15,938,344 (GRCm39) |
K535E |
probably damaging |
Het |
Ces1a |
A |
G |
8: 93,753,969 (GRCm39) |
Y345H |
probably damaging |
Het |
Col6a5 |
C |
A |
9: 105,741,347 (GRCm39) |
R2524I |
probably damaging |
Het |
Cracd |
A |
T |
5: 77,004,256 (GRCm39) |
I206F |
probably damaging |
Het |
Dctn1 |
G |
A |
6: 83,171,169 (GRCm39) |
R661H |
probably damaging |
Het |
Ddias |
T |
C |
7: 92,508,800 (GRCm39) |
T372A |
probably benign |
Het |
Dffb |
T |
C |
4: 154,049,976 (GRCm39) |
T296A |
probably damaging |
Het |
Dock8 |
A |
G |
19: 25,057,241 (GRCm39) |
Q216R |
probably benign |
Het |
Emx1 |
T |
C |
6: 85,165,237 (GRCm39) |
S105P |
probably benign |
Het |
Ep400 |
T |
C |
5: 110,867,102 (GRCm39) |
Y1014C |
unknown |
Het |
Fam193a |
A |
T |
5: 34,623,102 (GRCm39) |
K1230M |
possibly damaging |
Het |
Fgf9 |
A |
G |
14: 58,347,028 (GRCm39) |
Q207R |
probably benign |
Het |
Gm5460 |
G |
A |
14: 33,767,775 (GRCm39) |
C461Y |
possibly damaging |
Het |
Gpc1 |
T |
C |
1: 92,783,660 (GRCm39) |
I249T |
probably benign |
Het |
Htr1d |
T |
C |
4: 136,170,815 (GRCm39) |
I348T |
probably damaging |
Het |
Hyal4 |
A |
T |
6: 24,765,737 (GRCm39) |
S364C |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,897,275 (GRCm39) |
E1097G |
probably benign |
Het |
Igkv1-133 |
A |
T |
6: 67,701,944 (GRCm39) |
Q16L |
probably benign |
Het |
Kcnh5 |
A |
T |
12: 75,161,245 (GRCm39) |
I221N |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,760,263 (GRCm39) |
Y529H |
probably damaging |
Het |
Kyat1 |
T |
C |
2: 30,076,710 (GRCm39) |
H218R |
possibly damaging |
Het |
Lamb2 |
T |
G |
9: 108,357,758 (GRCm39) |
C94G |
probably damaging |
Het |
Met |
A |
T |
6: 17,549,085 (GRCm39) |
D979V |
probably damaging |
Het |
Midn |
A |
G |
10: 79,986,144 (GRCm39) |
D78G |
probably benign |
Het |
Myh1 |
A |
T |
11: 67,102,052 (GRCm39) |
M811L |
probably benign |
Het |
Myh7 |
T |
C |
14: 55,210,838 (GRCm39) |
E1693G |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,755,565 (GRCm39) |
T979A |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,384,807 (GRCm39) |
T733A |
probably damaging |
Het |
Ndufa9 |
A |
T |
6: 126,821,362 (GRCm39) |
M76K |
possibly damaging |
Het |
Nectin3 |
A |
G |
16: 46,215,542 (GRCm39) |
C74R |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,970,972 (GRCm39) |
F2514L |
probably damaging |
Het |
Or4a69 |
G |
A |
2: 89,313,471 (GRCm39) |
Q3* |
probably null |
Het |
Or52d3 |
T |
C |
7: 104,229,149 (GRCm39) |
S99P |
probably damaging |
Het |
Or5p81 |
CAAATA |
CA |
7: 108,266,869 (GRCm39) |
|
probably null |
Het |
P2ry2 |
A |
T |
7: 100,647,706 (GRCm39) |
S200T |
probably benign |
Het |
Pcdha5 |
G |
T |
18: 37,094,542 (GRCm39) |
M350I |
probably benign |
Het |
Pcdha5 |
G |
A |
18: 37,094,834 (GRCm39) |
V448M |
probably damaging |
Het |
Pex12 |
C |
T |
11: 83,188,455 (GRCm39) |
R180H |
possibly damaging |
Het |
Pip4p1 |
C |
G |
14: 51,167,749 (GRCm39) |
V59L |
probably damaging |
Het |
Pkd1l1 |
A |
T |
11: 8,912,701 (GRCm39) |
V168E |
probably damaging |
Het |
Prokr2 |
T |
A |
2: 132,223,095 (GRCm39) |
D149V |
probably damaging |
Het |
Rnf123 |
A |
G |
9: 107,940,720 (GRCm39) |
V707A |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,774,589 (GRCm39) |
E1189G |
probably damaging |
Het |
Scarf1 |
T |
C |
11: 75,406,117 (GRCm39) |
F134L |
probably damaging |
Het |
Sfxn5 |
A |
G |
6: 85,309,260 (GRCm39) |
|
probably null |
Het |
Shfl |
A |
T |
9: 20,784,473 (GRCm39) |
I186F |
possibly damaging |
Het |
Skic3 |
A |
G |
13: 76,330,986 (GRCm39) |
E1472G |
probably damaging |
Het |
Slc17a5 |
A |
T |
9: 78,445,556 (GRCm39) |
V433D |
probably damaging |
Het |
Snapc1 |
A |
G |
12: 74,011,417 (GRCm39) |
T28A |
probably benign |
Het |
Soat1 |
T |
C |
1: 156,258,669 (GRCm39) |
Y528C |
probably damaging |
Het |
Spem1 |
G |
A |
11: 69,712,344 (GRCm39) |
R107C |
possibly damaging |
Het |
Srcap |
T |
C |
7: 127,141,319 (GRCm39) |
S1639P |
probably damaging |
Het |
Sycp2 |
A |
T |
2: 178,016,388 (GRCm39) |
N691K |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,142,311 (GRCm39) |
I6183F |
probably damaging |
Het |
Tas2r110 |
A |
T |
6: 132,845,433 (GRCm39) |
M155L |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,693,305 (GRCm39) |
T1859I |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 130,030,809 (GRCm39) |
V1048D |
probably damaging |
Het |
Vav3 |
T |
C |
3: 109,248,482 (GRCm39) |
L43P |
probably damaging |
Het |
Vmn1r30 |
A |
T |
6: 58,412,437 (GRCm39) |
F132I |
probably benign |
Het |
Vmn2r24 |
A |
G |
6: 123,792,997 (GRCm39) |
R775G |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,883,189 (GRCm39) |
|
probably null |
Het |
Vps37c |
T |
A |
19: 10,683,569 (GRCm39) |
|
probably null |
Het |
Wwp2 |
A |
G |
8: 108,275,167 (GRCm39) |
D388G |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,355,336 (GRCm39) |
T3366S |
probably benign |
Het |
Zbtb49 |
A |
C |
5: 38,360,701 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Myo18b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Myo18b
|
APN |
5 |
113,021,997 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00847:Myo18b
|
APN |
5 |
112,978,255 (GRCm39) |
splice site |
probably benign |
|
IGL00848:Myo18b
|
APN |
5 |
113,019,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00969:Myo18b
|
APN |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
IGL01018:Myo18b
|
APN |
5 |
112,957,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01448:Myo18b
|
APN |
5 |
112,959,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Myo18b
|
APN |
5 |
112,957,566 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01556:Myo18b
|
APN |
5 |
112,905,315 (GRCm39) |
splice site |
probably benign |
|
IGL01637:Myo18b
|
APN |
5 |
112,988,495 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01819:Myo18b
|
APN |
5 |
113,025,916 (GRCm39) |
missense |
unknown |
|
IGL02007:Myo18b
|
APN |
5 |
113,022,838 (GRCm39) |
unclassified |
probably benign |
|
IGL02146:Myo18b
|
APN |
5 |
112,991,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02229:Myo18b
|
APN |
5 |
113,025,976 (GRCm39) |
missense |
unknown |
|
IGL02319:Myo18b
|
APN |
5 |
112,939,005 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02398:Myo18b
|
APN |
5 |
112,978,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02420:Myo18b
|
APN |
5 |
112,975,852 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02626:Myo18b
|
APN |
5 |
113,025,951 (GRCm39) |
missense |
unknown |
|
IGL02815:Myo18b
|
APN |
5 |
112,957,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Myo18b
|
APN |
5 |
112,923,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02852:Myo18b
|
APN |
5 |
112,863,377 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02995:Myo18b
|
APN |
5 |
112,923,279 (GRCm39) |
splice site |
probably benign |
|
IGL03019:Myo18b
|
APN |
5 |
112,840,263 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03039:Myo18b
|
APN |
5 |
112,988,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Myo18b
|
APN |
5 |
113,021,856 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03123:Myo18b
|
APN |
5 |
113,022,804 (GRCm39) |
unclassified |
probably benign |
|
IGL03288:Myo18b
|
APN |
5 |
112,937,863 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Myo18b
|
APN |
5 |
113,022,345 (GRCm39) |
unclassified |
probably benign |
|
klippel
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4651001:Myo18b
|
UTSW |
5 |
112,982,301 (GRCm39) |
missense |
probably benign |
0.01 |
R0271:Myo18b
|
UTSW |
5 |
112,957,551 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0277:Myo18b
|
UTSW |
5 |
112,841,213 (GRCm39) |
splice site |
probably benign |
|
R0352:Myo18b
|
UTSW |
5 |
113,022,389 (GRCm39) |
unclassified |
probably benign |
|
R0504:Myo18b
|
UTSW |
5 |
113,021,442 (GRCm39) |
unclassified |
probably benign |
|
R0539:Myo18b
|
UTSW |
5 |
112,871,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Myo18b
|
UTSW |
5 |
113,013,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Myo18b
|
UTSW |
5 |
112,946,700 (GRCm39) |
missense |
probably benign |
0.38 |
R0659:Myo18b
|
UTSW |
5 |
112,908,193 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0671:Myo18b
|
UTSW |
5 |
112,840,632 (GRCm39) |
missense |
probably benign |
0.00 |
R0847:Myo18b
|
UTSW |
5 |
113,022,354 (GRCm39) |
unclassified |
probably benign |
|
R1082:Myo18b
|
UTSW |
5 |
112,908,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Myo18b
|
UTSW |
5 |
112,951,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Myo18b
|
UTSW |
5 |
112,978,185 (GRCm39) |
missense |
probably benign |
0.12 |
R1280:Myo18b
|
UTSW |
5 |
112,871,671 (GRCm39) |
critical splice donor site |
probably null |
|
R1444:Myo18b
|
UTSW |
5 |
112,923,117 (GRCm39) |
critical splice donor site |
probably null |
|
R1446:Myo18b
|
UTSW |
5 |
112,905,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Myo18b
|
UTSW |
5 |
113,023,132 (GRCm39) |
nonsense |
probably null |
|
R1601:Myo18b
|
UTSW |
5 |
113,019,364 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1903:Myo18b
|
UTSW |
5 |
112,840,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R1936:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R2008:Myo18b
|
UTSW |
5 |
113,021,423 (GRCm39) |
missense |
probably benign |
|
R2127:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Myo18b
|
UTSW |
5 |
113,021,892 (GRCm39) |
missense |
probably benign |
0.01 |
R2170:Myo18b
|
UTSW |
5 |
112,871,724 (GRCm39) |
missense |
probably benign |
0.23 |
R2258:Myo18b
|
UTSW |
5 |
113,022,529 (GRCm39) |
unclassified |
probably benign |
|
R2265:Myo18b
|
UTSW |
5 |
112,930,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Myo18b
|
UTSW |
5 |
112,840,993 (GRCm39) |
missense |
probably benign |
0.01 |
R3160:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3777:Myo18b
|
UTSW |
5 |
112,905,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R4240:Myo18b
|
UTSW |
5 |
112,951,053 (GRCm39) |
critical splice donor site |
probably null |
|
R4243:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4245:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4533:Myo18b
|
UTSW |
5 |
112,840,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Myo18b
|
UTSW |
5 |
112,994,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Myo18b
|
UTSW |
5 |
113,023,041 (GRCm39) |
unclassified |
probably benign |
|
R4755:Myo18b
|
UTSW |
5 |
113,022,340 (GRCm39) |
nonsense |
probably null |
|
R4771:Myo18b
|
UTSW |
5 |
112,840,093 (GRCm39) |
nonsense |
probably null |
|
R4812:Myo18b
|
UTSW |
5 |
112,957,584 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4840:Myo18b
|
UTSW |
5 |
113,021,895 (GRCm39) |
missense |
probably benign |
0.02 |
R4888:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R4995:Myo18b
|
UTSW |
5 |
112,908,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R5001:Myo18b
|
UTSW |
5 |
112,909,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R5015:Myo18b
|
UTSW |
5 |
112,937,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Myo18b
|
UTSW |
5 |
113,023,083 (GRCm39) |
unclassified |
probably benign |
|
R5070:Myo18b
|
UTSW |
5 |
112,909,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5105:Myo18b
|
UTSW |
5 |
112,988,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R5130:Myo18b
|
UTSW |
5 |
113,021,769 (GRCm39) |
missense |
probably benign |
0.06 |
R5186:Myo18b
|
UTSW |
5 |
113,019,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Myo18b
|
UTSW |
5 |
112,905,439 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5535:Myo18b
|
UTSW |
5 |
112,937,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Myo18b
|
UTSW |
5 |
113,016,161 (GRCm39) |
missense |
probably damaging |
0.96 |
R5810:Myo18b
|
UTSW |
5 |
112,982,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Myo18b
|
UTSW |
5 |
112,950,196 (GRCm39) |
splice site |
probably null |
|
R6065:Myo18b
|
UTSW |
5 |
112,840,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Myo18b
|
UTSW |
5 |
113,022,157 (GRCm39) |
unclassified |
probably benign |
|
R6113:Myo18b
|
UTSW |
5 |
113,014,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Myo18b
|
UTSW |
5 |
113,022,038 (GRCm39) |
missense |
probably benign |
0.01 |
R6167:Myo18b
|
UTSW |
5 |
113,020,373 (GRCm39) |
splice site |
probably null |
|
R6220:Myo18b
|
UTSW |
5 |
112,905,373 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6276:Myo18b
|
UTSW |
5 |
112,959,508 (GRCm39) |
missense |
probably benign |
0.31 |
R6290:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6291:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6795:Myo18b
|
UTSW |
5 |
112,994,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Myo18b
|
UTSW |
5 |
112,909,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R6817:Myo18b
|
UTSW |
5 |
112,978,104 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Myo18b
|
UTSW |
5 |
112,950,258 (GRCm39) |
missense |
probably benign |
0.12 |
R7034:Myo18b
|
UTSW |
5 |
112,871,770 (GRCm39) |
nonsense |
probably null |
|
R7097:Myo18b
|
UTSW |
5 |
113,022,271 (GRCm39) |
missense |
unknown |
|
R7145:Myo18b
|
UTSW |
5 |
112,965,545 (GRCm39) |
nonsense |
probably null |
|
R7201:Myo18b
|
UTSW |
5 |
112,863,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Myo18b
|
UTSW |
5 |
112,923,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7265:Myo18b
|
UTSW |
5 |
112,959,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Myo18b
|
UTSW |
5 |
113,021,971 (GRCm39) |
missense |
probably benign |
0.25 |
R7466:Myo18b
|
UTSW |
5 |
112,871,758 (GRCm39) |
missense |
probably benign |
0.02 |
R7487:Myo18b
|
UTSW |
5 |
112,982,299 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7571:Myo18b
|
UTSW |
5 |
112,978,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Myo18b
|
UTSW |
5 |
113,025,969 (GRCm39) |
missense |
unknown |
|
R7612:Myo18b
|
UTSW |
5 |
113,013,168 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7617:Myo18b
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
R7696:Myo18b
|
UTSW |
5 |
112,840,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myo18b
|
UTSW |
5 |
113,022,891 (GRCm39) |
missense |
unknown |
|
R8047:Myo18b
|
UTSW |
5 |
112,871,681 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8070:Myo18b
|
UTSW |
5 |
112,938,986 (GRCm39) |
missense |
probably benign |
0.01 |
R8088:Myo18b
|
UTSW |
5 |
113,027,376 (GRCm39) |
start gained |
probably benign |
|
R8247:Myo18b
|
UTSW |
5 |
112,840,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Myo18b
|
UTSW |
5 |
112,943,273 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8313:Myo18b
|
UTSW |
5 |
113,023,045 (GRCm39) |
missense |
unknown |
|
R8375:Myo18b
|
UTSW |
5 |
112,908,259 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8432:Myo18b
|
UTSW |
5 |
112,912,378 (GRCm39) |
missense |
probably benign |
0.00 |
R8475:Myo18b
|
UTSW |
5 |
113,021,422 (GRCm39) |
nonsense |
probably null |
|
R8482:Myo18b
|
UTSW |
5 |
113,019,489 (GRCm39) |
nonsense |
probably null |
|
R8671:Myo18b
|
UTSW |
5 |
113,022,609 (GRCm39) |
missense |
unknown |
|
R8681:Myo18b
|
UTSW |
5 |
113,021,429 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8918:Myo18b
|
UTSW |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
R8941:Myo18b
|
UTSW |
5 |
113,022,795 (GRCm39) |
unclassified |
probably benign |
|
R8962:Myo18b
|
UTSW |
5 |
113,006,346 (GRCm39) |
missense |
probably benign |
0.24 |
R8972:Myo18b
|
UTSW |
5 |
112,841,164 (GRCm39) |
missense |
probably benign |
0.00 |
R9116:Myo18b
|
UTSW |
5 |
112,975,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Myo18b
|
UTSW |
5 |
113,022,927 (GRCm39) |
missense |
unknown |
|
R9358:Myo18b
|
UTSW |
5 |
112,943,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9469:Myo18b
|
UTSW |
5 |
112,994,247 (GRCm39) |
missense |
probably benign |
0.15 |
R9607:Myo18b
|
UTSW |
5 |
113,022,544 (GRCm39) |
missense |
unknown |
|
R9659:Myo18b
|
UTSW |
5 |
113,022,382 (GRCm39) |
missense |
unknown |
|
Z1088:Myo18b
|
UTSW |
5 |
112,905,350 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Myo18b
|
UTSW |
5 |
112,840,809 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Myo18b
|
UTSW |
5 |
112,979,056 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myo18b
|
UTSW |
5 |
112,957,604 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
113,021,407 (GRCm39) |
nonsense |
probably null |
|
Z1177:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
112,840,765 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo18b
|
UTSW |
5 |
113,023,018 (GRCm39) |
nonsense |
probably null |
|
|