Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
6 are Possibly Damaging.
7 are Probably Damaging.
11 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 8409 APN 1110017D15Rik 0.074 IGL00820 G1 4 41507178 L206Q A T missense Het probably damaging 1.000 phenotype 12/06/2012
2 8544 APN Abcg3 0.096 IGL00820 G1 5 104936012 I631F T A missense Het probably benign 0.017 phenotype 12/06/2012
3 9198 APN Baiap3 0.000 IGL00820 G1 17 25248690 D314G T C missense Het probably benign 0.201 phenotype 12/06/2012
4 9460 APN Ccl1 0.165 IGL00820 G1 11 82178088 E41G T C missense Het possibly damaging 0.850 phenotype 12/06/2012
5 10505 APN Ephx1 0.544 IGL00820 G1 1 180999821 Y89C T C missense Het possibly damaging 0.821 phenotype 12/06/2012
6 10738 APN Fbxw18 0.098 IGL00820 G1 9 109693369 T144I G A missense Het probably damaging 0.999 12/06/2012
7 10908 APN Galt 0.328 IGL00820 G1 4 41758570 A357V C T missense Het probably benign 0.016 phenotype 12/06/2012
8 10956 APN Gfra1 1.000 IGL00820 G1 19 58263905 T C splice site Het probably benign phenotype 12/06/2012
9 11278 APN Hivep1 0.555 IGL00820 G1 13 42183818 I2458L A T missense Het probably benign 0.287 phenotype 12/06/2012
10 11504 APN Itga8 0.622 IGL00820 G1 2 12232892 V339A A G missense Het possibly damaging 0.851 phenotype 12/06/2012
11 11664 APN Klk1b8 0.044 IGL00820 G1 7 43954786 I226T T C missense Het probably benign 0.398 phenotype 12/06/2012
12 11988 APN Mfsd6 0.114 IGL00820 G1 1 52708306 V467M C T missense Het probably damaging 1.000 12/06/2012
13 12080 APN Mrpl16 0.941 IGL00820 G1 19 11774413 V179A T C missense Het probably benign 0.016 phenotype 12/06/2012
14 12853 APN Olfr603 0.071 IGL00820 G1 7 103383465 T179I G A missense Het probably damaging 0.979 phenotype 12/06/2012
15 13079 APN Pnpla6 1.000 IGL00820 G1 8 3532358 T693A A G missense Het possibly damaging 0.955 phenotype 12/06/2012
16 13215 APN Ptpn2 0.000 IGL00820 G1 18 67675792 I318R A C missense Het possibly damaging 0.691 phenotype 12/06/2012
17 14046 APN Slc17a2 0.072 IGL00820 G1 13 23819334 H285R A G missense Het probably benign 0.127 12/06/2012
18 277992 APN Slit2 1.000 IGL00820 G1 5 47989151 E95K G A missense Het possibly damaging 0.877 phenotype 04/16/2015
19 14217 APN Sptb 0.644 IGL00820 G1 12 76632477 L68P A G missense Het probably damaging 1.000 phenotype 12/06/2012
20 14294 APN Stxbp6 0.093 IGL00820 G1 12 44861346 T163I G A missense Het probably damaging 0.974 phenotype 12/06/2012
21 14432 APN Tex15 0.564 IGL00820 G1 8 33579006 A G splice site Het probably benign phenotype 12/06/2012
22 14638 APN Tti1 0.959 IGL00820 G1 2 158008968 E117G T C missense Het probably damaging 1.000 12/06/2012
23 14679 APN Ube4b 1.000 IGL00820 G1 4 149352921 T C splice site Het probably benign phenotype 12/06/2012
24 14867 APN Wipi1 0.466 IGL00820 G1 11 109583119 A C splice site Het probably benign phenotype 12/06/2012
25 14901 APN Zan 0.065 IGL00820 G1 5 137386364 C5133S A T missense Het unknown phenotype 12/06/2012
[records 1 to 25 of 25]