Incidental Mutations

9 incidental mutations are currently displayed, and affect 9 genes.
1 are Possibly Damaging.
4 are Probably Damaging.
4 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 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 289773 APN Bbs4 0.559 IGL02278 9 59341168 Q84L T A missense Het possibly damaging 0.638 phenotype 04/16/2015
2 289771 APN Cemip 0.084 IGL02278 7 83937438 W1303R A T missense Het probably damaging 1.000 phenotype 04/16/2015
3 289769 APN Edrf1 0.678 IGL02278 7 133657000 S702P T C missense Het probably benign 0.001 phenotype 04/16/2015
4 289767 APN Muc4 0.099 IGL02278 16 32754529 H1468N C A missense Het probably benign 0.015 0.090 phenotype 04/16/2015
5 289775 APN Nav1 0.939 IGL02278 1 135463714 G A splice site Het probably benign phenotype 04/16/2015
6 289770 APN Pramel5 0.132 IGL02278 4 144271551 L374P A G missense Het probably damaging 1.000 04/16/2015
7 289772 APN Slc2a2 1.000 IGL02278 3 28717455 I178T T C missense Het probably damaging 0.994 phenotype 04/16/2015
8 289774 APN Tsnaxip1 0.539 IGL02278 8 105827781 A G utr 5 prime Het probably benign 04/16/2015
9 289768 APN Zfp850 0.074 IGL02278 7 28008397 Q7L T A missense Het probably damaging 0.960 04/16/2015
[records 1 to 9 of 9]