Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
4 are Possibly Damaging.
11 are Probably Damaging.
8 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 25 of 25] 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 8606 APN Adh4 0.105 IGL00592 G1 3 138420636 I91V A G missense Het probably damaging 0.987 phenotype 12/06/2012
2 4247 APN Ak6 0.967 IGL00592 G1 13 100664091 V74A T C missense Het probably benign 0.055 phenotype 04/20/2012
3 8972 APN Antxr1 0.000 IGL00592 G1 6 87288802 V110F C A missense Het probably damaging 1.000 phenotype 12/06/2012
4 8976 APN Anxa1 0.354 IGL00592 G1 19 20377669 D247G T C missense Het probably benign 0.009 phenotype 12/06/2012
5 3993 APN Dgkg 0.174 IGL00592 G1 16 22479362 T C splice site Het probably benign phenotype 04/20/2012
6 10562 APN Eva1b 0.087 IGL00592 G1 4 126149650 M161T T C missense Het probably benign 0.021 12/06/2012
7 4812 APN Fbxw22 0.055 IGL00592 G1 9 109384040 V280F C A missense Het possibly damaging 0.675 04/20/2012
8 6635 APN Klhl9 0.000 IGL00592 G1 4 88721141 S288P A G missense Het probably damaging 0.991 phenotype 04/20/2012
9 6523 APN Masp2 0.141 IGL00592 G1 4 148602729 P23S C T missense Het probably benign 0.053 phenotype 04/20/2012
10 12280 APN Ncam1 0.917 IGL00592 G1 9 49523565 D600V T A missense Het probably damaging 1.000 phenotype 12/06/2012
11 5982 APN Pcnx4 0.130 IGL00592 G1 12 72579365 N1115S A G missense Het probably damaging 0.973 04/20/2012
12 3890 APN Pdia2 0.112 IGL00592 G1 17 26198116 V109A A G missense Het probably damaging 0.983 phenotype 04/20/2012
13 332737 APN Pla1a 0.055 IGL00592 G1 16 38414850 H161N G T missense Het probably damaging 0.999 phenotype 08/05/2015
14 7020 APN Prokr2 0.203 IGL00592 G1 2 132381504 D39E A T missense Het probably benign 0.284 phenotype 04/20/2012
15 332738 APN Sall4 1.000 IGL00592 G1 2 168755963 D319G T C missense Het probably damaging 1.000 phenotype 08/05/2015
16 14005 APN Sgms2 0.173 IGL00592 G1 3 131341833 S131P A G missense Het possibly damaging 0.911 phenotype 12/06/2012
17 14054 APN Slc22a2 0.000 IGL00592 G1 17 12608418 Q319L A T missense Het possibly damaging 0.792 phenotype 12/06/2012
18 14076 APN Slc27a5 0.164 IGL00592 G1 7 12988639 I636T A G missense Het probably benign 0.084 phenotype 12/06/2012
19 5362 APN Tas2r131 0.000 IGL00592 G1 6 132957196 T217P T G missense Het probably damaging 0.995 04/20/2012
20 14564 APN Trh 0.000 IGL00592 G1 6 92242742 M198V T C missense Het possibly damaging 0.775 phenotype 12/06/2012
21 4604 APN Ube2b 0.501 IGL00592 G1 11 51986719 V141G A C missense Het probably damaging 1.000 phenotype 04/20/2012
22 7136 APN Ube2l6 0.084 IGL00592 G1 2 84809029 V112E T A missense Het probably damaging 1.000 phenotype 04/20/2012
23 14791 APN Vmn1r79 0.070 IGL00592 G1 7 12177007 I272T T C missense Het probably benign 0.047 12/06/2012
24 14892 APN Xylb 0.085 IGL00592 G1 9 119390483 Q513* C T nonsense Het probably null phenotype 12/06/2012
25 14905 APN Zbtb4 0.000 IGL00592 G1 11 69776731 C287* T A nonsense Het probably null 12/06/2012
[records 1 to 25 of 25]