Incidental Mutations

9 incidental mutations are currently displayed, and affect 9 genes.
1 are Possibly Damaging.
3 are Probably Damaging.
3 are Probably Benign.
2 are Probably Null.
2 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 94545 UTSW Ahr 0.955 R1133 G1 225 N 12 35526806 L42P A G missense Het probably damaging 1.000 phenotype 01/05/2014
2 94517 UTSW B430305J03Rik 0.382 R1133 G1 225 N 3 61364009 W105* C T nonsense Het probably null 01/05/2014
3 94561 UTSW Gpr156 0.000 R1133 G1 225 N 16 38005321 N633K T A missense Het probably benign 0.104 phenotype 01/05/2014
4 94529 UTSW Hook2 0.286 R1133 G1 225 N 8 84995804 L324P T C missense Het probably damaging 1.000 phenotype 01/05/2014
5 94532 UTSW Olfr147 0.057 R1133 G1 225 N 9 38403731 M283L A T missense Het probably benign 0.003 phenotype 01/05/2014
6 94553 UTSW Socs4 0.361 R1133 G1 225 N 14 47290194 I195M A G missense Het probably benign 0.006 phenotype 01/05/2014
7 94540 UTSW Syne1 1.000 R1133 G1 225 N 10 5349044 I1014T A G missense Het possibly damaging 0.774 phenotype 01/05/2014
8 94513 UTSW Ttc30a2 0.000 R1133 G1 191 N 2 75977383 Q262* G A nonsense Het probably null 01/05/2014
9 94523 UTSW Ugt2b38 0.060 R1133 G1 225 N 5 87412373 N361H T G missense Het probably damaging 1.000 0.862 01/05/2014
[records 1 to 9 of 9]