Incidental Mutations

41 incidental mutations are currently displayed, and affect 41 genes.
7 are Possibly Damaging.
14 are Probably Damaging.
16 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 41 of 41] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 1445 APN 9030624J02Rik 0.163 IGL00159 G1 7 118797047 (GRCm38) G A critical splice donor site 1 bp Het probably null 2011-07-12
2 821 APN Axin1 1.000 IGL00159 G1 17 26142805 (GRCm38) D41V A T missense Het possibly damaging 0.883 phenotype 2011-07-12
3 306564 APN BC034090 0.058 IGL00159 G1 1 155225451 (GRCm38) E718* C A nonsense Het probably null 2015-04-16
4 1924 APN Cdc123 1.000 IGL00159 G1 2 5804935 (GRCm38) Q222K G T missense Het probably benign 0.011 2011-07-12
5 1629 APN Clip1 0.000 IGL00159 G1 5 123603654 (GRCm38) V1053G A C missense Het possibly damaging 0.945 phenotype 2011-07-12
6 1721 APN Dock7 0.000 IGL00159 G1 4 99063985 (GRCm38) E416V T A missense Het probably damaging 0.996 phenotype 2011-07-12
7 306565 APN Dydc1 0.072 IGL00159 G1 14 41087413 (GRCm38) L143P T C missense Het probably damaging 1.000 phenotype 2015-04-16
8 1351 APN Dync2h1 1.000 IGL00159 G1 9 7158839 (GRCm38) V732A A G missense Het probably benign 0.421 phenotype 2011-07-12
9 306567 APN Dzip1l 0.331 IGL00159 G1 9 99637777 (GRCm38) L119Q T A missense Het probably damaging 0.991 2015-04-16
10 1548 APN Erp27 0.130 IGL00159 G1 6 136909502 (GRCm38) S178C T A missense Het probably damaging 0.999 phenotype 2011-07-12
11 1848 APN Fbn1 0.941 IGL00159 G1 2 125397873 (GRCm38) V298A A G missense Het probably benign 0.139 phenotype 2011-07-12
12 969 APN Fbxo34 0.072 IGL00159 G1 14 47529474 (GRCm38) H97R A G missense Het probably damaging 0.966 phenotype 2011-07-12
13 965 APN Gm20521 IGL00159 G1 14 54884622 (GRCm38) Q81* C T nonsense Het probably null 2011-07-12
14 870 APN Gspt1 0.964 IGL00159 G1 16 11222612 (GRCm38) M610V T C missense Het probably damaging 0.992 2011-07-12
15 1301 APN Herc1 0.000 IGL00159 G1 9 66437682 (GRCm38) Q1919R A G missense Het possibly damaging 0.939 phenotype 2011-07-12
16 1957 APN Il19 0.056 IGL00159 G1 1 130935055 (GRCm38) A G splice site Het probably benign phenotype 2011-07-12
17 306563 APN Kif14 0.902 IGL00159 G1 1 136469018 (GRCm38) S354N G A missense Het probably benign 0.112 phenotype 2015-04-16
18 894 APN Lrrk2 0.572 IGL00159 G1 15 91747799 (GRCm38) K1309E A G missense Het possibly damaging 0.905 phenotype 2011-07-12
19 1711 APN Lurap1 0.067 IGL00159 G1 4 116137690 (GRCm38) T115A T C missense Het probably damaging 0.980 2011-07-12
20 1637 APN Myo18b 1.000 IGL00159 G1 5 112874131 (GRCm38) T465K G T missense Het probably benign 0.055 phenotype 2011-07-12
21 306568 APN Nwd1 0.175 IGL00159 G1 8 72671077 (GRCm38) D648V A T missense Het probably damaging 0.989 phenotype 2015-04-16
22 1734 APN Olfr272 0.051 IGL00159 G1 4 52911618 (GRCm38) M59L T G missense Het possibly damaging 0.955 phenotype 2011-07-12
23 1469 APN Olfr520 0.220 IGL00159 G1 7 99735317 (GRCm38) R58H G A missense Het probably benign 0.004 phenotype 2011-07-12
24 1666 APN Otof 0.154 IGL00159 G1 5 30375904 (GRCm38) Y1527C T C missense Het probably damaging 0.997 phenotype 2011-07-12
25 1106 APN Otop3 0.062 IGL00159 G1 11 115344397 (GRCm38) C285Y G A missense Het probably damaging 0.999 2011-07-12
26 1280 APN Parp3 0.000 IGL00159 G1 9 106471387 (GRCm38) I478T A G missense Het probably benign 0.000 phenotype 2011-07-12
27 933 APN Pdzd2 0.140 IGL00159 G1 15 12457983 (GRCm38) E265K C T missense Het possibly damaging 0.929 phenotype 2011-07-12
28 306566 APN Pik3c2g 0.079 IGL00159 G1 6 139896125 (GRCm38) L634P T C missense Het probably damaging 1.000 phenotype 2015-04-16
29 707 APN Prkg1 0.507 IGL00159 G1 19 31302340 (GRCm38) V165L C A missense Het probably benign 0.021 phenotype 2011-07-12
30 756 APN Riok3 0.230 IGL00159 G1 18 12148891 (GRCm38) I306V A G missense Het possibly damaging 0.810 phenotype 2011-07-12
31 1022 APN Ror2 1.000 IGL00159 G1 13 53113082 (GRCm38) D439G T C missense Het probably benign 0.012 phenotype 2011-07-12
32 1891 APN Scn2a 1.000 IGL00159 G1 2 65743090 (GRCm38) I1428N T A missense Het probably damaging 1.000 phenotype 2011-07-12
33 949 APN Sgcg 0.168 IGL00159 G1 14 61232475 (GRCm38) D146N C T missense Het probably benign 0.003 phenotype 2011-07-12
34 1239 APN Slc16a9 0.000 IGL00159 G1 10 70282699 (GRCm38) R283G A G missense Het probably benign 0.042 2011-07-12
35 1072 APN Sptb 0.819 IGL00159 G1 12 76621331 (GRCm38) D664G T C missense Het probably benign 0.002 phenotype 2011-07-12
36 810 APN Tmprss3 0.086 IGL00159 G1 17 31195008 (GRCm38) D54V T A missense Het probably damaging 0.968 phenotype 2011-07-12
37 1008 APN Ttc37 0.405 IGL00159 G1 13 76143278 (GRCm38) T C critical splice donor site 2 bp Het probably null phenotype 2011-07-12
38 1143 APN Tubd1 0.950 IGL00159 G1 11 86565729 (GRCm38) V374F G T missense Het probably benign 0.068 2011-07-12
39 1503 APN Vmn2r57 0.125 IGL00159 G1 7 41428785 (GRCm38) M83K A T missense Het probably benign 0.000 2011-07-12
40 1298 APN Vps13c 0.000 IGL00159 G1 9 67945999 (GRCm38) E2458G A G missense Het probably benign 0.198 phenotype 2011-07-12
41 922 APN Zhx2 0.252 IGL00159 G1 15 57822870 (GRCm38) E545V A T missense Het probably damaging 1.000 phenotype 2011-07-12
[records 1 to 41 of 41]