Incidental Mutations

13 incidental mutations are currently displayed, and affect 13 genes.
2 are Possibly Damaging.
3 are Probably Damaging.
5 are Probably Benign.
3 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 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 12445 APN Adipor2 0.201 IGL00639 G1 6 119370168 C51* A T nonsense Het probably null phenotype 12/06/2012
2 12483 APN Atmin 1.000 IGL00639 G1 8 116956657 D352G A G missense Het probably damaging 0.998 phenotype 12/06/2012
3 12538 APN Cntln 0.281 IGL00639 G1 4 85006434 E592G A G missense Het probably benign 0.251 12/06/2012
4 277841 APN Crygd 0.269 IGL00639 G1 1 65062091 R115Q C T missense Het probably benign 0.321 phenotype 04/16/2015
5 12676 APN Il31ra 0.000 IGL00639 G1 13 112549559 Y65* A T nonsense Het probably null phenotype 12/06/2012
6 12726 APN Megf8 0.930 IGL00639 G1 7 25343684 F1344L T C missense Het possibly damaging 0.866 phenotype 12/06/2012
7 12926 APN Pcdh18 0.000 IGL00639 G1 3 49755616 I417V T C missense Het probably benign 0.343 phenotype 12/06/2012
8 13183 APN Prpf4b 1.000 IGL00639 G1 13 34899173 N844S A G missense Het possibly damaging 0.704 phenotype 12/06/2012
9 14261 APN Stard13 0.000 IGL00639 G1 5 151042239 E917G T C missense Het probably damaging 1.000 phenotype 12/06/2012
10 14431 APN Tex15 0.428 IGL00639 G1 8 33575311 S1590P T C missense Het probably benign 0.183 phenotype 12/06/2012
11 277842 APN Thrap3 0.928 IGL00639 G1 4 126165578 G892S C T missense Het probably benign 0.006 04/16/2015
12 14817 APN Vrk1 0.818 IGL00639 G1 12 106055916 T A splice site 6 bp Het probably null phenotype 12/06/2012
13 14989 APN Zfp655 0.437 IGL00639 G1 5 145244145 Y271C A G missense Het probably damaging 1.000 phenotype 12/06/2012
[records 1 to 13 of 13]