Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
5 are Possibly Damaging.
8 are Probably Damaging.
8 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 21 of 21] 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 102856 APN Alk 0.139 IGL01652 G1 17 72603531 V60E A T missense Het probably damaging 0.999 phenotype 01/21/2014
2 102859 APN Ank2 1.000 IGL01652 G1 3 126933041 K868R T C missense Het probably benign 0.001 phenotype 01/21/2014
3 102854 APN Ankrd13a 0.119 IGL01652 G1 5 114791336 D158V A T missense Het probably damaging 1.000 01/21/2014
4 102857 APN Arhgap12 0.000 IGL01652 G1 18 6061853 N380K G T missense Het possibly damaging 0.889 phenotype 01/21/2014
5 102863 APN Cpn1 0.000 IGL01652 G1 19 43986094 F65L A T missense Het possibly damaging 0.799 phenotype 01/21/2014
6 102851 APN Dlec1 0.000 IGL01652 G1 9 119143907 H1496Q T A missense Het probably benign 0.013 phenotype 01/21/2014
7 102869 APN Dock1 1.000 IGL01652 G1 7 134777497 C T splice site Het probably benign phenotype 01/21/2014
8 102852 APN Dok1 0.156 IGL01652 G1 6 83032562 N143D T C missense Het probably damaging 0.999 phenotype 01/21/2014
9 102864 APN Fcmr 0.000 IGL01652 G1 1 130878507 P363L C T missense Het probably benign 0.246 phenotype 01/21/2014
10 102865 APN Galk2 0.000 IGL01652 G1 2 125896765 T171A A G missense Het probably benign 0.289 phenotype 01/21/2014
11 102855 APN Hrh3 0.276 IGL01652 G1 2 180101103 P244Q G T missense Het possibly damaging 0.685 phenotype 01/21/2014
12 102858 APN Icam1 0.130 IGL01652 G1 9 21019176 Y109H T C missense Het probably damaging 1.000 phenotype 01/21/2014
13 102866 APN Nup93 0.908 IGL01652 G1 8 94296559 V132A T C missense Het possibly damaging 0.932 phenotype 01/21/2014
14 102850 APN Olfr1218 0.054 IGL01652 G1 2 89054569 Y286N A T missense Het probably damaging 1.000 phenotype 01/21/2014
15 102861 APN Pla2g4f 0.051 IGL01652 G1 2 120302235 I707V T C missense Het possibly damaging 0.863 01/21/2014
16 102868 APN Rpgrip1 0.305 IGL01652 G1 14 52145492 G A unclassified Het probably benign phenotype 01/21/2014
17 102862 APN Sbf2 0.340 IGL01652 G1 7 110447120 V290E A T missense Het probably damaging 1.000 phenotype 01/21/2014
18 102867 APN Stard3 0.000 IGL01652 G1 11 98378733 T G splice site Het probably benign phenotype 01/21/2014
19 332104 APN Sufu 1.000 IGL01652 G1 19 46475620 Y424H T C missense Het probably damaging 1.000 phenotype 08/05/2015
20 102860 APN Trim35 0.075 IGL01652 G1 14 66308801 V339G T G missense Het probably damaging 0.996 phenotype 01/21/2014
21 102853 APN Vmn1r80 0.107 IGL01652 G1 7 12193136 I58V A G missense Het probably benign 0.193 01/21/2014
[records 1 to 21 of 21]