Incidental Mutations

9 incidental mutations are currently displayed, and affect 9 genes.
0 are Possibly Damaging.
6 are Probably Damaging.
1 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 9 of 9] 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 416197 APN Gm6614 0.076 IGL03300 6 141994806 F110L A G missense Het probably damaging 0.963 08/02/2016
2 416204 APN Lpar5 0.116 IGL03300 6 125082240 L308P T C missense Het probably damaging 1.000 phenotype 08/02/2016
3 416202 APN Mcm9 0.000 IGL03300 10 53611427 S515P A G missense Het probably damaging 0.999 phenotype 08/02/2016
4 416198 APN Olfr1258 0.061 IGL03300 2 89930227 C139* T A nonsense Het probably null phenotype 08/02/2016
5 416199 APN Olfr716 0.112 IGL03300 7 107147409 F31S T C missense Het probably damaging 1.000 phenotype 08/02/2016
6 416200 APN Pclo 0.000 IGL03300 5 14712798 M3762V A G missense Het unknown phenotype 08/02/2016
7 416201 APN Pgr 0.493 IGL03300 9 8961539 D871N G A missense Het probably damaging 0.998 phenotype 08/02/2016
8 416203 APN Ppfibp1 0.531 IGL03300 6 147030327 E957G A G missense Het probably damaging 1.000 phenotype 08/02/2016
9 416205 APN Pus10 0.000 IGL03300 11 23731368 T C utr 3 prime Het probably benign phenotype 08/02/2016
[records 1 to 9 of 9]