Incidental Mutations

11 incidental mutations are currently displayed, and affect 11 genes.
2 are Possibly Damaging.
2 are Probably Damaging.
6 are Probably Benign.
1 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 11 of 11] 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 9138 APN Atp6v0a1 0.818 IGL00687 G1 11 101030505 T A critical splice donor site 2 bp Het probably null phenotype 12/06/2012
2 9860 APN Cpb2 0.198 IGL00687 G1 14 75275093 I315M A G missense Het possibly damaging 0.640 phenotype 12/06/2012
3 10212 APN Dnah11 0.514 IGL00687 G1 12 117922004 T A splice site Het probably benign phenotype 12/06/2012
4 10862 APN G3bp2 0.787 IGL00687 G1 5 92065848 E150G T C missense Het probably damaging 0.978 12/06/2012
5 11390 APN Ibsp 0.484 IGL00687 G1 5 104310068 E157G A G missense Het probably benign 0.269 phenotype 12/06/2012
6 10338 APN Ms4a4c 0.031 IGL00687 G1 19 11421318 S167P T C missense Het possibly damaging 0.938 12/06/2012
7 13023 APN Pkhd1 0.250 IGL00687 G1 1 20524070 N1273S T C missense Het probably benign 0.193 phenotype 12/06/2012
8 13749 APN Rap1gap2 0.449 IGL00687 G1 11 74416259 D337V T A missense Het probably benign 0.252 phenotype 12/06/2012
9 14088 APN Slc35f3 0.176 IGL00687 G1 8 126382164 F151L T C missense Het probably benign 0.023 12/06/2012
10 14719 APN Unc5d 0.309 IGL00687 G1 8 28715813 A T splice site Het probably benign phenotype 12/06/2012
11 277853 APN Zfp711 IGL00687 G1 X 112624811 R284Q G A missense Het probably damaging 0.998 phenotype 04/16/2015
[records 1 to 11 of 11]