Incidental Mutations

13 incidental mutations are currently displayed, and affect 13 genes.
5 are Possibly Damaging.
6 are Probably Damaging.
2 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 13 of 13] 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 12435 APN Acp1 0.132 IGL00722 G1 12 30897793 D82G T C missense Het probably damaging 0.999 phenotype 12/06/2012
2 12456 APN Alpk1 0.000 IGL00722 G1 3 127680213 S714P A G missense Het probably benign 0.003 phenotype 12/06/2012
3 12484 APN Atp11b 0.270 IGL00722 G1 3 35819935 I491T T C missense Het probably damaging 0.999 phenotype 12/06/2012
4 12427 APN Frg2f1 0.103 IGL00722 G1 4 119531110 R64K C T missense Het possibly damaging 0.837 12/06/2012
5 12664 APN Hibch 0.280 IGL00722 G1 1 52901320 V216A T C missense Het probably damaging 0.964 phenotype 12/06/2012
6 12736 APN Mttp 0.835 IGL00722 G1 3 138109015 V500F C A missense Het possibly damaging 0.838 phenotype 12/06/2012
7 12878 APN Osbpl9 0.000 IGL00722 G1 4 109072010 I397V T C missense Het probably damaging 0.995 phenotype 12/06/2012
8 13867 APN Rpusd4 0.936 IGL00722 G1 9 35268418 V69D T A missense Het possibly damaging 0.656 12/06/2012
9 13990 APN Setd2 0.916 IGL00722 G1 9 110551136 S1340P T C missense Het possibly damaging 0.937 phenotype 12/06/2012
10 14269 APN Stk17b 0.130 IGL00722 G1 1 53764140 S167G T C missense Het probably damaging 0.994 phenotype 12/06/2012
11 14286 APN Strn 0.655 IGL00722 G1 17 78692420 D129G T C missense Het possibly damaging 0.889 phenotype 12/06/2012
12 14839 APN Wdr44 0.594 IGL00722 G1 X 23732309 T C intron Het probably benign phenotype 12/06/2012
13 14979 APN Zfp558 0.000 IGL00722 G1 9 18456521 P324T G T missense Het probably damaging 0.971 12/06/2012
[records 1 to 13 of 13]