Incidental Mutations

24 incidental mutations are currently displayed, and affect 24 genes.
5 are Possibly Damaging.
5 are Probably Damaging.
8 are Probably Benign.
6 are Probably Null.
2 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 24 of 24] 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 153859 APN Ankrd17 1.000 IGL01776 G1 5 90283364 Q854* G A nonsense Het probably null phenotype 02/04/2014
2 153873 APN Armc8 0.802 IGL01776 G1 9 99526883 A G splice site Het probably benign 02/04/2014
3 153861 APN Chrna7 0.000 IGL01776 G1 7 63099519 V405A A G missense Het probably benign 0.012 phenotype 02/04/2014
4 153875 APN Col8a2 0.500 IGL01776 G1 4 126309805 C A unclassified Het probably benign phenotype 02/04/2014
5 153857 APN Dcn 0.000 IGL01776 G1 10 97495076 I91V A G missense Het possibly damaging 0.884 phenotype 02/04/2014
6 153867 APN Dock7 0.000 IGL01776 G1 4 98940941 R2069S T A missense Het possibly damaging 0.654 phenotype 02/04/2014
7 153856 APN Gm7247 0.165 IGL01776 G1 14 51521899 S112G A G missense Het possibly damaging 0.863 02/04/2014
8 153863 APN Hmcn1 0.000 IGL01776 G1 1 150672038 T2721P T G missense Het possibly damaging 0.699 phenotype 02/04/2014
9 153865 APN Hsd3b3 0.093 IGL01776 G1 3 98743847 T96A T C missense Het probably benign 0.048 02/04/2014
10 153866 APN Ifi207 0.080 IGL01776 G1 1 173725044 L936F G A missense Het probably damaging 0.997 02/04/2014
11 153869 APN Kcp 0.209 IGL01776 G1 6 29497908 P477S G A missense Het probably damaging 0.998 phenotype 02/04/2014
12 153871 APN Mei1 0.206 IGL01776 G1 15 82095932 T C critical splice donor site 2 bp Het probably null phenotype 02/04/2014
13 153870 APN Mgmt 0.000 IGL01776 G1 7 137121564 L121* T A nonsense Het probably null phenotype 02/04/2014
14 153868 APN Mrps35 0.955 IGL01776 G1 6 147070716 V286I G A missense Het probably benign 0.326 phenotype 02/04/2014
15 153874 APN Naxd 0.455 IGL01776 G1 8 11505525 T C splice site 6 bp Het probably null 02/04/2014
16 153878 APN Pam 1.000 IGL01776 G1 1 97885600 A G critical splice donor site 2 bp Het probably null phenotype 02/04/2014
17 153877 APN Plcxd1 0.108 IGL01776 G1 5 110101380 G A splice site Het probably benign 02/04/2014
18 153872 APN Rasgrp1 0.414 IGL01776 G1 2 117286840 A G critical splice donor site 2 bp Het probably null phenotype 02/04/2014
19 153876 APN Spag9 0.811 IGL01776 G1 11 94116727 C T splice site Het probably benign phenotype 02/04/2014
20 153858 APN Spire2 0.122 IGL01776 G1 8 123359392 S288P T C missense Het probably damaging 0.980 02/04/2014
21 153860 APN Stk11ip 1.000 IGL01776 G1 1 75527821 V322A T C missense Het probably benign 0.020 02/04/2014
22 153864 APN Syt17 0.000 IGL01776 G1 7 118409953 L343R A C missense Het probably damaging 0.990 02/04/2014
23 153862 APN Tap1 0.000 IGL01776 G1 17 34193128 V436I G A missense Het possibly damaging 0.820 phenotype 02/04/2014
24 278884 APN Virma 1.000 IGL01776 G1 4 11527792 R1228C C T missense Het probably damaging 1.000 04/16/2015
[records 1 to 24 of 24]