Incidental Mutations

9 incidental mutations are currently displayed, and affect 9 genes.
1 are Possibly Damaging.
3 are Probably Damaging.
5 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 9 of 9] 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 9016 APN Arhgap11a 0.000 IGL00869 G1 2 113834826 T476A T C missense Het probably damaging 0.990 phenotype 12/06/2012
2 9170 APN AW551984 0.081 IGL00869 G1 9 39593434 A G splice site Het probably benign 12/06/2012
3 10944 APN Gcn1l1 0.948 IGL00869 G1 5 115588143 T A splice site Het probably benign 12/06/2012
4 278041 APN Hnrnpm 1.000 IGL00869 G1 17 33649902 R517L C A missense Het probably damaging 0.988 phenotype 04/16/2015
5 11442 APN Il1f6 0.055 IGL00869 G1 2 24216580 T59A A G missense Het probably benign 0.209 phenotype 12/06/2012
6 12783 APN Nrm 0.787 IGL00869 G1 17 35864755 H251R A G missense Het probably benign 0.065 phenotype 12/06/2012
7 14190 APN Sp7 1.000 IGL00869 G1 15 102358651 A240E G T missense Het probably benign 0.036 phenotype 12/06/2012
8 14207 APN Speer4b 0.086 IGL00869 G1 5 27498718 K141R T C missense Het probably damaging 0.987 12/06/2012
9 14488 APN Tmem132c 0.235 IGL00869 G1 5 127563242 H826Y C T missense Het possibly damaging 0.948 12/06/2012
[records 1 to 9 of 9]