Incidental Mutations

18 incidental mutations are currently displayed, and affect 18 genes.
2 are Possibly Damaging.
7 are Probably Damaging.
5 are Probably Benign.
4 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 18 of 18] 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 28321 APN Ahi1 0.853 IGL00914 G1 10 20984299 T G splice site Het probably null phenotype 04/17/2013
2 28508 APN Aipl1 0.133 IGL00914 G1 11 72031547 D112G T C missense Het probably damaging 1.000 phenotype 04/17/2013
3 27230 APN Casz1 1.000 IGL00914 G1 4 148929371 E131K G A missense Het probably damaging 0.999 phenotype 04/17/2013
4 26864 APN Chrna4 0.162 IGL00914 G1 2 181029031 Y311H A G missense Het probably damaging 1.000 phenotype 04/17/2013
5 29048 APN Cyp2d34 0.081 IGL00914 G1 15 82620714 N48K G T missense Het probably damaging 0.976 04/17/2013
6 28145 APN Dnajc13 0.932 IGL00914 G1 9 104212882 K696I T A missense Het possibly damaging 0.896 phenotype 04/17/2013
7 28320 APN Fbxo30 0.272 IGL00914 G1 10 11290539 V335A T C missense Het probably benign 0.014 phenotype 04/17/2013
8 29049 APN Itga5 1.000 IGL00914 G1 15 103350372 A G critical splice donor site 2 bp Het probably null phenotype 04/17/2013
9 28511 APN Morc2a 1.000 IGL00914 G1 11 3668844 G A splice site 5 bp Het probably null phenotype 04/17/2013
10 28509 APN Nek8 0.861 IGL00914 G1 11 78173075 I35V T C missense Het possibly damaging 0.796 phenotype 04/17/2013
11 29495 APN Olfr1453 0.087 IGL00914 G1 19 13027591 V246A A G missense Het probably damaging 0.977 phenotype 04/17/2013
12 28144 APN Olfr893 0.077 IGL00914 G1 9 38209799 A G intron Het probably null phenotype 04/17/2013
13 28510 APN Pcyt2 1.000 IGL00914 G1 11 120614325 A G unclassified Het probably benign phenotype 04/17/2013
14 26865 APN Sec23b 1.000 IGL00914 G1 2 144566864 S156R T G missense Het probably damaging 0.998 phenotype 04/17/2013
15 28837 APN Shc3 0.110 IGL00914 G1 13 51480227 T A splice site Het probably benign phenotype 04/17/2013
16 28717 APN Sntg2 0.102 IGL00914 G1 12 30257957 A G intron Het probably benign phenotype 04/17/2013
17 26863 APN Srms 0.811 IGL00914 G1 2 181207772 M280L T A missense Het probably benign 0.019 phenotype 04/17/2013
18 28716 APN Wdr60 1.000 IGL00914 G1 12 116232603 V508A A G missense Het probably damaging 0.998 phenotype 04/17/2013
[records 1 to 18 of 18]