Incidental Mutations

23 incidental mutations are currently displayed, and affect 22 genes.
6 are Possibly Damaging.
10 are Probably Damaging.
5 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 23 of 23] 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 92402 APN Adamts5 0.212 IGL01616 G1 16 85887814 T A splice site 3 bp Het probably null phenotype 12/09/2013
2 92394 APN Afg3l1 0.080 IGL01616 G1 8 123502007 W771R T A missense Het probably damaging 1.000 phenotype 12/09/2013
3 92392 APN Braf 1.000 IGL01616 G1 6 39651652 S348P A G missense Het probably damaging 1.000 phenotype 12/09/2013
4 92386 APN Cd200 0.070 IGL01616 G1 16 45397056 T112A T C missense Het possibly damaging 0.900 phenotype 12/09/2013
5 92383 APN Cep350 0.957 IGL01616 G1 1 155953247 I304V T C missense Het probably benign 0.001 phenotype 12/09/2013
6 92390 APN Fry 0.679 IGL01616 G1 5 150399599 T1072A A G missense Het probably damaging 0.998 12/09/2013
7 92401 APN Fry 0.679 IGL01616 G1 5 150438811 A T splice site 3 bp Het probably null 12/09/2013
8 92396 APN Fuk 0.214 IGL01616 G1 8 110890476 H388N G T missense Het possibly damaging 0.745 phenotype 12/09/2013
9 92403 APN Gcdh 0.000 IGL01616 G1 8 84893659 G8D C T missense Het probably damaging 0.997 phenotype 12/09/2013
10 92393 APN Ivns1abp 0.419 IGL01616 G1 1 151361543 T486K C A missense Het possibly damaging 0.688 phenotype 12/09/2013
11 92397 APN Mat1a 0.126 IGL01616 G1 14 41109479 V55M G A missense Het probably damaging 1.000 phenotype 12/09/2013
12 92391 APN Olfr656 0.076 IGL01616 G1 7 104617721 F22S T C missense Het probably damaging 0.980 phenotype 12/09/2013
13 92404 APN Pcnx3 0.000 IGL01616 G1 19 5667259 C T unclassified Het probably benign 12/09/2013
14 92398 APN Psrc1 0.509 IGL01616 G1 3 108386692 S275Y C A missense Het possibly damaging 0.931 phenotype 12/09/2013
15 92384 APN Ptpn21 0.134 IGL01616 G1 12 98680013 L1062P A G missense Het probably damaging 1.000 phenotype 12/09/2013
16 92400 APN Slc22a13b-ps IGL01616 G1 9 119220928 A C critical splice acceptor site Het probably benign 12/09/2013
17 92395 APN Slc35b1 0.946 IGL01616 G1 11 95389084 M178K T A missense Het probably benign 0.012 phenotype 12/09/2013
18 92387 APN Slc6a11 1.000 IGL01616 G1 6 114134868 Q132L A T missense Het possibly damaging 0.931 phenotype 12/09/2013
19 92382 APN Slc9a8 0.000 IGL01616 G1 2 167424166 T21I C T missense Het possibly damaging 0.461 phenotype 12/09/2013
20 92385 APN Tox 0.000 IGL01616 G1 4 6688430 T526A T C missense Het probably damaging 0.987 phenotype 12/09/2013
21 92388 APN Ubr3 1.000 IGL01616 G1 2 70020484 P1749S C T missense Het probably benign 0.138 phenotype 12/09/2013
22 92389 APN Wdfy3 0.938 IGL01616 G1 5 101913260 A1363S C A missense Het probably damaging 0.966 phenotype 12/09/2013
23 92381 APN Zdhhc23 0.000 IGL01616 G1 16 43973480 H277L T A missense Het probably damaging 1.000 12/09/2013
[records 1 to 23 of 23]