Incidental Mutations

49 incidental mutations are currently displayed, and affect 49 genes.
12 are Possibly Damaging.
18 are Probably Damaging.
14 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 49 of 49] 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 74709 APN 1110004E09Rik 0.163 IGL01338 G1 16 90926048 N266S T C missense Het possibly damaging 0.596 phenotype 10/07/2013
2 74727 APN Adam23 1.000 IGL01338 G1 1 63551855 T494A A G missense Het possibly damaging 0.505 phenotype 10/07/2013
3 74714 APN Adamts16 0.000 IGL01338 G1 13 70836115 C143Y C T missense Het probably damaging 1.000 phenotype 10/07/2013
4 74687 APN Cacna1i 0.000 IGL01338 G1 15 80348380 I195V A G missense Het probably damaging 0.993 phenotype 10/07/2013
5 74696 APN Casp7 0.000 IGL01338 G1 19 56404464 S17P T C missense Het probably benign 0.000 phenotype 10/07/2013
6 278288 APN Cox6a1 0.336 IGL01338 G1 5 115345839 C A unclassified Het probably benign phenotype 04/16/2015
7 74725 APN Cpvl 0.088 IGL01338 G1 6 53974655 S48C T A missense Het possibly damaging 0.923 phenotype 10/07/2013
8 74695 APN Cyp2b19 0.056 IGL01338 G1 7 26759417 M138I G T missense Het probably benign 0.094 10/07/2013
9 74718 APN Dennd5a 0.101 IGL01338 G1 7 109919404 Y510C T C missense Het possibly damaging 0.920 phenotype 10/07/2013
10 74704 APN Derl2 1.000 IGL01338 G1 11 71010355 F229S A G missense Het possibly damaging 0.613 phenotype 10/07/2013
11 74717 APN Dlec1 0.000 IGL01338 G1 9 119120911 E452G A G missense Het probably damaging 1.000 phenotype 10/07/2013
12 74721 APN Dsc2 0.000 IGL01338 G1 18 20047157 K180E T C missense Het probably benign 0.192 phenotype 10/07/2013
13 74693 APN Dus1l 0.116 IGL01338 G1 11 120793092 R177C G A missense Het possibly damaging 0.950 10/07/2013
14 74713 APN Egfr 0.896 IGL01338 G1 11 16863020 I167V A G missense Het probably damaging 0.996 phenotype 10/07/2013
15 74729 APN Fam219b 0.061 IGL01338 G1 9 57538022 A T critical splice acceptor site Het probably null 10/07/2013
16 74699 APN Fn1 1.000 IGL01338 G1 1 71626210 E916G T C missense Het probably damaging 0.978 phenotype 10/07/2013
17 74686 APN Gm2058 IGL01338 G1 7 39589156 C T exon Het noncoding transcript 10/07/2013
18 74715 APN Gpd1 0.000 IGL01338 G1 15 99718175 V22E T A missense Het probably damaging 0.984 phenotype 10/07/2013
19 74692 APN Hsf2 0.000 IGL01338 G1 10 57501379 F124L T C missense Het probably damaging 1.000 phenotype 10/07/2013
20 74707 APN I0C0044D17Rik 0.391 IGL01338 G1 4 98820099 A G unclassified Het probably benign 10/07/2013
21 74712 APN Igfbp3 0.000 IGL01338 G1 11 7208478 F262I A T missense Het possibly damaging 0.688 phenotype 10/07/2013
22 74726 APN Klhl18 0.000 IGL01338 G1 9 110455433 Y62H A G missense Het probably damaging 1.000 10/07/2013
23 74711 APN Lama2 0.335 IGL01338 G1 10 27188272 E1238K C T missense Het probably benign 0.127 phenotype 10/07/2013
24 74701 APN Man1b1 0.000 IGL01338 G1 2 25338227 K170E A G missense Het probably benign 0.013 phenotype 10/07/2013
25 74723 APN Mcrs1 1.000 IGL01338 G1 15 99249501 I39N A T missense Het probably damaging 0.996 phenotype 10/07/2013
26 74728 APN Mug2 0.066 IGL01338 G1 6 122049628 T C splice site Het probably benign 10/07/2013
27 74702 APN Neu3 0.052 IGL01338 G1 7 99813422 G365W C A missense Het probably damaging 1.000 phenotype 10/07/2013
28 74730 APN Nipal3 0.098 IGL01338 G1 4 135471883 A C critical splice donor site 2 bp Het probably null phenotype 10/07/2013
29 74703 APN Nrxn3 0.000 IGL01338 G1 12 89255034 I528V A G missense Het possibly damaging 0.861 phenotype 10/07/2013
30 74685 APN Olfr122 0.065 IGL01338 G1 17 37771839 H71L A T missense Het possibly damaging 0.902 phenotype 10/07/2013
31 74708 APN Osbpl8 0.260 IGL01338 G1 10 111267747 K204R A G missense Het probably damaging 0.989 phenotype 10/07/2013
32 74724 APN Pax8 1.000 IGL01338 G1 2 24435919 S318P A G missense Het possibly damaging 0.930 phenotype 10/07/2013
33 74710 APN Pcdh18 0.000 IGL01338 G1 3 49756141 N242Y T A missense Het probably damaging 1.000 phenotype 10/07/2013
34 74719 APN Pkd1l2 0.000 IGL01338 G1 8 117059520 K649* T A nonsense Het probably null phenotype 10/07/2013
35 74720 APN Ppm1n 0.150 IGL01338 G1 7 19279254 D257E A T missense Het probably benign 0.037 10/07/2013
36 74705 APN Pxdn 0.496 IGL01338 G1 12 30002797 E811G A G missense Het probably damaging 1.000 phenotype 10/07/2013
37 278287 APN Relb 0.923 IGL01338 G1 7 19616373 I218V T C missense Het probably benign 0.026 phenotype 04/16/2015
38 74716 APN Rreb1 0.944 IGL01338 G1 13 37931034 C790R T C missense Het probably benign 0.091 phenotype 10/07/2013
39 74691 APN Rtkn2 0.129 IGL01338 G1 10 68025519 C258F G T missense Het possibly damaging 0.835 10/07/2013
40 74731 APN Scn11a 0.090 IGL01338 G1 9 119784161 G A splice site Het probably benign phenotype 10/07/2013
41 74697 APN Snx8 0.000 IGL01338 G1 5 140358096 R96C G A missense Het probably damaging 1.000 10/07/2013
42 74722 APN Syne2 0.346 IGL01338 G1 12 76060226 T5649S A T missense Het possibly damaging 0.550 phenotype 10/07/2013
43 74690 APN Tm2d3 1.000 IGL01338 G1 7 65695222 C82* T A nonsense Het probably null phenotype 10/07/2013
44 74698 APN Tnpo2 0.000 IGL01338 G1 8 85040526 L55P T C missense Het probably damaging 0.981 10/07/2013
45 74694 APN Tsc22d2 0.412 IGL01338 G1 3 58417415 T C unclassified Het probably benign 10/07/2013
46 74700 APN Ttll3 0.000 IGL01338 G1 6 113394729 V19G T G missense Het probably damaging 1.000 phenotype 10/07/2013
47 74689 APN Ube2r2 0.266 IGL01338 G1 4 41174119 I86V A G missense Het probably benign 0.270 phenotype 10/07/2013
48 74706 APN Vps13d 1.000 IGL01338 G1 4 145088322 T3153I G A missense Het probably damaging 0.995 phenotype 10/07/2013
49 74688 APN Wwp1 0.000 IGL01338 G1 4 19627636 I753T A G missense Het probably damaging 1.000 phenotype 10/07/2013
[records 1 to 49 of 49]