Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
3 are Possibly Damaging.
4 are Probably Damaging.
13 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 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 29043 APN 5031439G07Rik 0.091 IGL00910 G1 15 84955819 L109P A G missense Het probably damaging 0.999 04/17/2013
2 27398 APN Aacs 0.586 IGL00910 G1 5 125508708 M316K T A missense Het probably benign 0.001 04/17/2013
3 28833 APN Adarb2 0.000 IGL00910 G1 13 8672433 V375A T C missense Het probably damaging 0.999 phenotype 04/17/2013
4 28003 APN Adgra2 1.000 IGL00910 G1 8 27085983 A13E C A missense Het possibly damaging 0.815 phenotype 04/17/2013
5 28138 APN Ankrd34c 0.063 IGL00910 G1 9 89729026 S421T A T missense Het probably benign 0.147 04/17/2013
6 26852 APN Bpifa6 0.083 IGL00910 G1 2 153990466 M298L A T missense Het probably benign 0.001 04/17/2013
7 27079 APN Casq2 0.000 IGL00910 G1 3 102110231 T C splice site Het probably benign phenotype 04/17/2013
8 26851 APN Ckap5 1.000 IGL00910 G1 2 91576050 T762A A G missense Het probably benign 0.323 phenotype 04/17/2013
9 28002 APN Dhx38 0.962 IGL00910 G1 8 109559034 V389A A G missense Het probably benign 0.074 phenotype 04/17/2013
10 26621 APN Dnah7b 0.107 IGL00910 G1 1 46066729 A T unclassified Het probably benign 04/17/2013
11 28501 APN Dnajc7 0.000 IGL00910 G1 11 100599191 F79L A T missense Het possibly damaging 0.901 phenotype 04/17/2013
12 26620 APN Dyrk3 0.250 IGL00910 G1 1 131136336 I3T A G missense Het possibly damaging 0.921 phenotype 04/17/2013
13 28709 APN Fam84a 0.115 IGL00910 G1 12 14150526 S67G T C missense Het probably benign 0.141 04/17/2013
14 27787 APN Fchsd2 0.197 IGL00910 G1 7 101277626 I641T T C missense Het probably benign 0.003 04/17/2013
15 27788 APN Furin 1.000 IGL00910 G1 7 80390996 V698A A G missense Het probably benign 0.000 phenotype 04/17/2013
16 28834 APN Prl2c5 0.095 IGL00910 G1 13 13189476 G A critical splice donor site 1 bp Het probably null 04/17/2013
17 26853 APN Ryr3 0.514 IGL00910 G1 2 112728934 A T splice site Het probably benign phenotype 04/17/2013
18 28711 APN Serpina6 0.076 IGL00910 G1 12 103651965 G T unclassified Het probably benign phenotype 04/17/2013
19 28001 APN Slc6a2 0.225 IGL00910 G1 8 92996100 Y575C A G missense Het probably damaging 1.000 phenotype 04/17/2013
20 28710 APN Trim9 0.305 IGL00910 G1 12 70347113 E19G T C missense Het probably damaging 0.981 phenotype 04/17/2013
21 28315 APN Tsfm 1.000 IGL00910 G1 10 127028359 G T intron Het probably benign phenotype 04/17/2013
[records 1 to 21 of 21]