Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810459M11Rik |
C |
A |
1: 85,974,166 (GRCm39) |
T161K |
probably benign |
Het |
Actn3 |
G |
A |
19: 4,914,539 (GRCm39) |
R530W |
probably damaging |
Het |
Alg11 |
C |
T |
8: 22,558,026 (GRCm39) |
A404V |
possibly damaging |
Het |
Alkbh8 |
T |
A |
9: 3,369,751 (GRCm39) |
V340D |
probably damaging |
Het |
Arhgef12 |
T |
C |
9: 42,886,364 (GRCm39) |
H1166R |
probably benign |
Het |
Aspm |
T |
A |
1: 139,398,269 (GRCm39) |
D978E |
possibly damaging |
Het |
Bod1l |
C |
T |
5: 41,975,815 (GRCm39) |
G1833D |
probably damaging |
Het |
Brd3 |
A |
G |
2: 27,339,251 (GRCm39) |
V676A |
possibly damaging |
Het |
Brip1 |
G |
A |
11: 86,037,009 (GRCm39) |
T454I |
possibly damaging |
Het |
C3ar1 |
T |
C |
6: 122,827,723 (GRCm39) |
I165V |
probably benign |
Het |
Camta1 |
T |
A |
4: 151,228,864 (GRCm39) |
Q656L |
probably benign |
Het |
Casp14 |
A |
T |
10: 78,549,178 (GRCm39) |
L256* |
probably null |
Het |
Cdh23 |
G |
T |
10: 60,255,556 (GRCm39) |
H773Q |
possibly damaging |
Het |
Chd1 |
G |
T |
17: 15,989,016 (GRCm39) |
D1590Y |
probably damaging |
Het |
Chd1 |
G |
A |
17: 15,989,015 (GRCm39) |
W1589* |
probably null |
Het |
Cldn19 |
A |
G |
4: 119,112,951 (GRCm39) |
Q61R |
probably damaging |
Het |
Cyp2a22 |
A |
G |
7: 26,631,949 (GRCm39) |
S436P |
probably benign |
Het |
Emc10 |
A |
C |
7: 44,142,051 (GRCm39) |
V124G |
probably damaging |
Het |
Enam |
A |
T |
5: 88,650,885 (GRCm39) |
D723V |
probably benign |
Het |
Eps8 |
C |
A |
6: 137,504,128 (GRCm39) |
Q158H |
probably damaging |
Het |
Ercc6 |
G |
A |
14: 32,263,253 (GRCm39) |
D486N |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,703,885 (GRCm39) |
E1485G |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,169,844 (GRCm39) |
K2972E |
probably benign |
Het |
Fbxw28 |
T |
C |
9: 109,168,602 (GRCm39) |
K30R |
probably null |
Het |
Flot2 |
T |
A |
11: 77,948,339 (GRCm39) |
L164Q |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,779,739 (GRCm39) |
I162L |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,815,815 (GRCm39) |
L3849F |
probably benign |
Het |
Gabrb1 |
C |
G |
5: 71,858,154 (GRCm39) |
P60R |
probably damaging |
Het |
Galnt14 |
T |
C |
17: 73,811,893 (GRCm39) |
R443G |
probably benign |
Het |
Gas8 |
C |
T |
8: 124,257,753 (GRCm39) |
T400M |
probably benign |
Het |
Gfap |
T |
C |
11: 102,785,214 (GRCm39) |
Y254C |
probably damaging |
Het |
Git2 |
A |
G |
5: 114,883,543 (GRCm39) |
S396P |
probably damaging |
Het |
Glb1l3 |
A |
T |
9: 26,740,349 (GRCm39) |
M327K |
probably benign |
Het |
Gm10715 |
A |
C |
9: 3,038,062 (GRCm39) |
|
probably benign |
Het |
Gm10787 |
G |
A |
10: 76,857,841 (GRCm39) |
|
noncoding transcript |
Het |
Gm1123 |
T |
A |
9: 98,900,622 (GRCm39) |
D78V |
probably damaging |
Het |
Gm27013 |
T |
C |
6: 130,655,079 (GRCm39) |
T128A |
probably benign |
Het |
Gpbp1 |
A |
G |
13: 111,577,164 (GRCm39) |
|
probably null |
Het |
Gphn |
G |
A |
12: 78,569,729 (GRCm39) |
|
probably null |
Het |
Gpr157 |
A |
G |
4: 150,186,823 (GRCm39) |
E317G |
probably benign |
Het |
Gsdmc4 |
T |
A |
15: 63,765,596 (GRCm39) |
M318L |
probably benign |
Het |
Gtf2f2 |
A |
T |
14: 76,248,131 (GRCm39) |
W19R |
probably damaging |
Het |
Gvin-ps3 |
T |
C |
7: 105,680,627 (GRCm39) |
|
noncoding transcript |
Het |
Helb |
A |
G |
10: 119,920,763 (GRCm39) |
V1060A |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,895,778 (GRCm39) |
G1596D |
probably benign |
Het |
Il1rl2 |
T |
C |
1: 40,366,547 (GRCm39) |
I27T |
possibly damaging |
Het |
Inpp5j |
A |
G |
11: 3,449,676 (GRCm39) |
V702A |
probably damaging |
Het |
Kmt2d |
A |
C |
15: 98,759,775 (GRCm39) |
V1161G |
unknown |
Het |
Krtap1-3 |
T |
G |
11: 99,481,715 (GRCm39) |
Y144S |
possibly damaging |
Het |
Layn |
C |
T |
9: 50,968,682 (GRCm39) |
V354M |
probably damaging |
Het |
Lrba |
G |
A |
3: 86,526,816 (GRCm39) |
|
probably null |
Het |
Lrp8 |
T |
A |
4: 107,727,234 (GRCm39) |
L893Q |
possibly damaging |
Het |
Mrps9 |
T |
A |
1: 42,937,575 (GRCm39) |
|
probably benign |
Het |
Mug1 |
T |
A |
6: 121,862,813 (GRCm39) |
M1387K |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,618,091 (GRCm39) |
E2321G |
probably benign |
Het |
Nrsn2 |
C |
T |
2: 152,211,552 (GRCm39) |
V160I |
probably benign |
Het |
Nup210 |
G |
A |
6: 91,008,650 (GRCm39) |
Q510* |
probably null |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or2ag12 |
T |
G |
7: 106,277,330 (GRCm39) |
D121A |
probably damaging |
Het |
P3h3 |
G |
T |
6: 124,827,600 (GRCm39) |
Q479K |
possibly damaging |
Het |
Paqr9 |
T |
A |
9: 95,442,723 (GRCm39) |
F238I |
probably damaging |
Het |
Parp3 |
A |
T |
9: 106,350,308 (GRCm39) |
L343H |
probably damaging |
Het |
Pcdh18 |
A |
C |
3: 49,699,117 (GRCm39) |
M1115R |
probably damaging |
Het |
Pcdh8 |
A |
G |
14: 80,008,308 (GRCm39) |
V85A |
possibly damaging |
Het |
Pcdhb4 |
A |
G |
18: 37,441,452 (GRCm39) |
N254S |
possibly damaging |
Het |
Pld1 |
T |
C |
3: 28,130,700 (GRCm39) |
V500A |
probably benign |
Het |
Pramel29 |
T |
C |
4: 143,935,144 (GRCm39) |
K199R |
probably damaging |
Het |
Prkg2 |
A |
T |
5: 99,129,002 (GRCm39) |
D311E |
probably benign |
Het |
Prss42 |
T |
C |
9: 110,628,369 (GRCm39) |
L171P |
probably damaging |
Het |
Pth2 |
T |
A |
7: 44,830,767 (GRCm39) |
L17H |
probably damaging |
Het |
Reln |
A |
T |
5: 22,223,844 (GRCm39) |
|
probably null |
Het |
Rmi2 |
G |
T |
16: 10,657,701 (GRCm39) |
V104L |
probably damaging |
Het |
Rpusd4 |
T |
A |
9: 35,179,831 (GRCm39) |
V108D |
probably damaging |
Het |
Rufy4 |
C |
A |
1: 74,168,198 (GRCm39) |
T82K |
possibly damaging |
Het |
Scimp |
G |
A |
11: 70,682,294 (GRCm39) |
Q141* |
probably null |
Het |
Sel1l2 |
T |
C |
2: 140,105,390 (GRCm39) |
T267A |
probably benign |
Het |
Sema5a |
T |
A |
15: 32,550,400 (GRCm39) |
S146R |
possibly damaging |
Het |
Sh2d3c |
T |
C |
2: 32,611,172 (GRCm39) |
M1T |
probably null |
Het |
Slc30a6 |
T |
C |
17: 74,712,716 (GRCm39) |
L71P |
probably damaging |
Het |
Srrm3 |
A |
G |
5: 135,883,449 (GRCm39) |
Y224C |
possibly damaging |
Het |
Tacr3 |
A |
T |
3: 134,560,615 (GRCm39) |
T185S |
possibly damaging |
Het |
Tas2r140 |
T |
A |
6: 133,032,528 (GRCm39) |
T77S |
probably benign |
Het |
Thsd7b |
T |
C |
1: 129,523,581 (GRCm39) |
V128A |
probably benign |
Het |
Tnfrsf10b |
T |
G |
14: 70,013,608 (GRCm39) |
H179Q |
probably damaging |
Het |
Tonsl |
A |
G |
15: 76,517,409 (GRCm39) |
V770A |
probably benign |
Het |
Trim42 |
G |
A |
9: 97,244,982 (GRCm39) |
P606L |
probably benign |
Het |
Trim45 |
A |
T |
3: 100,832,804 (GRCm39) |
T346S |
possibly damaging |
Het |
Ttc28 |
C |
A |
5: 111,433,947 (GRCm39) |
S2296Y |
probably damaging |
Het |
Ttc41 |
C |
T |
10: 86,566,989 (GRCm39) |
R552C |
probably benign |
Het |
Tube1 |
A |
G |
10: 39,020,842 (GRCm39) |
N243D |
probably benign |
Het |
Tvp23b |
G |
T |
11: 62,770,424 (GRCm39) |
|
probably null |
Het |
Ubxn11 |
T |
A |
4: 133,836,919 (GRCm39) |
I49N |
probably damaging |
Het |
Usp17le |
T |
A |
7: 104,418,977 (GRCm39) |
E55V |
probably benign |
Het |
Vmn2r114 |
A |
T |
17: 23,510,353 (GRCm39) |
V709D |
probably damaging |
Het |
Vmn2r129 |
G |
C |
4: 156,685,733 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r23 |
C |
T |
6: 123,690,033 (GRCm39) |
T303M |
probably damaging |
Het |
Vmn2r60 |
C |
T |
7: 41,785,285 (GRCm39) |
P166S |
probably damaging |
Het |
Vmn2r83 |
A |
G |
10: 79,313,682 (GRCm39) |
I97V |
possibly damaging |
Het |
Wbp2nl |
A |
T |
15: 82,198,537 (GRCm39) |
K358M |
possibly damaging |
Het |
Xpo1 |
T |
A |
11: 23,228,183 (GRCm39) |
I150N |
probably damaging |
Het |
Zfp113 |
G |
A |
5: 138,143,687 (GRCm39) |
L188F |
probably damaging |
Het |
Zfp189 |
T |
G |
4: 49,529,984 (GRCm39) |
S362R |
probably damaging |
Het |
Zfp593os |
A |
G |
4: 133,972,587 (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 |
R2483:Myo18b
|
UTSW |
5 |
113,006,274 (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 |
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 |
|
|