Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
7 are Possibly Damaging.
4 are Probably Damaging.
9 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 413307 APN Bmp7 1.000 IGL03211 2 172872883 V378I C T missense Het possibly damaging 0.696 phenotype 08/02/2016
2 413317 APN Cd209b 0.062 IGL03211 8 3918830 G T splice site Het probably benign phenotype 08/02/2016
3 413312 APN Cilp 0.000 IGL03211 9 65280175 Q1184L A T missense Het probably benign 0.000 phenotype 08/02/2016
4 413302 APN Cysltr2 0.060 IGL03211 14 73029715 M185K A T missense Het possibly damaging 0.901 phenotype 08/02/2016
5 413298 APN Dcaf6 0.000 IGL03211 1 165422933 F121L A G missense Het possibly damaging 0.549 08/02/2016
6 413305 APN Dnajc8 1.000 IGL03211 4 132544737 Y95N T A missense Het possibly damaging 0.949 08/02/2016
7 413309 APN Ebf3 1.000 IGL03211 7 137231304 V214A A G missense Het probably benign 0.211 phenotype 08/02/2016
8 413310 APN Elavl3 0.448 IGL03211 9 22018678 V310A A G missense Het probably damaging 1.000 phenotype 08/02/2016
9 413299 APN Emc2 0.908 IGL03211 15 43507672 R131* C T nonsense Het probably null 08/02/2016
10 413311 APN Hcn4 1.000 IGL03211 9 58858151 V639M G A missense Het unknown phenotype 08/02/2016
11 413301 APN Kif21a 1.000 IGL03211 15 90997963 D46A T G missense Het possibly damaging 0.729 phenotype 08/02/2016
12 413297 APN Kitl 0.285 IGL03211 10 100080859 S175P T C missense Het probably benign 0.187 phenotype 08/02/2016
13 413320 APN Klhl32 0.084 IGL03211 4 24792616 C T critical splice donor site 1 bp Het probably null 08/02/2016
14 413308 APN Plcg1 1.000 IGL03211 2 160759691 T972I C T missense Het possibly damaging 0.819 phenotype 08/02/2016
15 413314 APN Prdm13 0.000 IGL03211 4 21678492 H666R T C missense Het probably damaging 0.998 phenotype 08/02/2016
16 413319 APN Rap1gap 0.000 IGL03211 4 137715846 G A critical splice donor site 1 bp Het probably null phenotype 08/02/2016
17 413296 APN Rdh7 0.094 IGL03211 10 127887623 N121S T C missense Het probably benign 0.008 08/02/2016
18 413300 APN Ric8b 1.000 IGL03211 10 85001793 I488N T A missense Het probably damaging 1.000 08/02/2016
19 413316 APN Slc38a2 0.368 IGL03211 15 96698272 A T splice site Het probably null 08/02/2016
20 413318 APN Slc9a9 0.000 IGL03211 9 95137990 G A splice site Het probably benign phenotype 08/02/2016
21 413306 APN Tk2 0.712 IGL03211 8 104243441 I64F T A missense Het probably damaging 1.000 phenotype 08/02/2016
22 413303 APN Virma 1.000 IGL03211 4 11548770 W1776* G A nonsense Het probably null 08/02/2016
23 413313 APN Vrk1 0.807 IGL03211 12 106036588 A15V C T missense Het probably benign 0.030 phenotype 08/02/2016
24 413321 APN Wdfy3 0.899 IGL03211 5 101844912 T C splice site Het probably benign phenotype 08/02/2016
25 413304 APN Wfdc10 0.082 IGL03211 2 164657252 V94A T C missense Het probably benign 0.346 08/02/2016
26 413315 APN Zfp780b 0.064 IGL03211 7 27963175 C652S A T missense Het possibly damaging 0.931 08/02/2016
[records 1 to 26 of 26]