Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
7 are Possibly Damaging.
13 are Probably Damaging.
13 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 37 of 37] 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 75956 APN 2310002L09Rik 0.064 IGL01366 G1 4 73950700 A T utr 5 prime Het probably benign 10/07/2013
2 75925 APN Adamts2 0.119 IGL01366 G1 11 50796468 Y1041H T C missense Het probably damaging 0.998 phenotype 10/07/2013
3 75929 APN Adck5 0.000 IGL01366 G1 15 76595616 *568C A C makesense Het probably null 10/07/2013
4 75957 APN AK157302 0.941 IGL01366 G1 13 21495301 T A utr 5 prime Het probably benign 10/07/2013
5 75953 APN Bmpr2 1.000 IGL01366 G1 1 59813677 G56W G T missense Het probably damaging 0.999 phenotype 10/07/2013
6 75932 APN Capn11 0.000 IGL01366 G1 17 45653200 I146S A C missense Het probably damaging 1.000 phenotype 10/07/2013
7 75949 APN Ccdc162 0.069 IGL01366 G1 10 41580306 D1613E A T missense Het possibly damaging 0.490 10/07/2013
8 75943 APN Ccdc167 0.085 IGL01366 G1 17 29705312 E50G T C missense Het probably damaging 1.000 10/07/2013
9 75947 APN Col5a2 1.000 IGL01366 G1 1 45391888 P864Q G T missense Het possibly damaging 0.456 phenotype 10/07/2013
10 75954 APN Col7a1 1.000 IGL01366 G1 9 108977119 C T splice site Het probably benign phenotype 10/07/2013
11 75952 APN Crebbp 1.000 IGL01366 G1 16 4126506 H556L T A missense Het probably damaging 0.999 phenotype 10/07/2013
12 75930 APN Dcpp1 0.139 IGL01366 G1 17 23882736 I153N T A missense Het possibly damaging 0.900 10/07/2013
13 75931 APN Dgke 0.217 IGL01366 G1 11 89055386 R196H C T missense Het probably benign 0.254 phenotype 10/07/2013
14 75951 APN Efr3a 0.267 IGL01366 G1 15 65851150 I459K T A missense Het probably benign 0.365 phenotype 10/07/2013
15 75939 APN Espl1 1.000 IGL01366 G1 15 102319836 C1682S T A missense Het probably benign 0.001 phenotype 10/07/2013
16 75934 APN Exosc3 0.964 IGL01366 G1 4 45317747 R185H C T missense Het probably damaging 0.996 phenotype 10/07/2013
17 75940 APN Fam160b2 0.085 IGL01366 G1 14 70585373 R688C G A missense Het probably damaging 1.000 10/07/2013
18 75926 APN Fgd6 0.566 IGL01366 G1 10 94043476 V64A T C missense Het possibly damaging 0.712 10/07/2013
19 75928 APN Gata3 1.000 IGL01366 G1 2 9877465 L42P A G missense Het probably damaging 0.996 phenotype 10/07/2013
20 75927 APN Ggta1 0.000 IGL01366 G1 2 35402450 E282* C A nonsense Het probably null phenotype 10/07/2013
21 75944 APN Ghr 0.000 IGL01366 G1 15 3320187 D503G T C missense Het probably damaging 1.000 phenotype 10/07/2013
22 278316 APN Gls 1.000 IGL01366 G1 1 52168399 G602D C T missense Het probably damaging 1.000 phenotype 04/16/2015
23 75924 APN Gm2058 IGL01366 G1 7 39589234 A G exon Het noncoding transcript 10/07/2013
24 75955 APN Grb7 0.000 IGL01366 G1 11 98452274 T C unclassified Het probably benign phenotype 10/07/2013
25 75938 APN Ifngr1 0.000 IGL01366 G1 10 19609600 H449L A T missense Het probably damaging 1.000 phenotype 10/07/2013
26 75935 APN Ighg2b 0.129 IGL01366 G1 12 113307036 D158A T G missense Het possibly damaging 0.793 10/07/2013
27 75937 APN Nphs2 0.155 IGL01366 G1 1 156311035 V83A T C missense Het probably benign 0.394 phenotype 10/07/2013
28 75950 APN Parp6 0.470 IGL01366 G1 9 59636713 M390K T A missense Het possibly damaging 0.748 10/07/2013
29 75948 APN Pask 0.213 IGL01366 G1 1 93310852 K1304E T C missense Het probably benign 0.016 phenotype 10/07/2013
30 75941 APN Scai 0.613 IGL01366 G1 2 39106961 S274P A G missense Het probably benign 0.362 phenotype 10/07/2013
31 75946 APN Sik2 0.797 IGL01366 G1 9 50907463 S404P A G missense Het probably damaging 0.965 phenotype 10/07/2013
32 75936 APN Slc7a8 0.531 IGL01366 G1 14 54781188 I47N A T missense Het probably damaging 1.000 phenotype 10/07/2013
33 75933 APN Tas2r113 0.071 IGL01366 G1 6 132893797 I263F A T missense Het probably benign 0.062 10/07/2013
34 75942 APN Tdrd1 0.579 IGL01366 G1 19 56855302 D737E T A missense Het probably benign 0.001 phenotype 10/07/2013
35 75945 APN Trio 1.000 IGL01366 G1 15 27732868 T2976A T C missense Het possibly damaging 0.759 phenotype 10/07/2013
36 75958 APN Ttc28 0.000 IGL01366 G1 5 111085171 T C critical splice donor site 2 bp Het probably null 10/07/2013
37 75923 APN Vmn1r21 0.360 IGL01366 G1 6 57843814 I215T A G missense Het probably benign 0.007 10/07/2013
[records 1 to 37 of 37]