Incidental Mutations

38 incidental mutations are currently displayed, and affect 37 genes.
9 are Possibly Damaging.
15 are Probably Damaging.
12 are Probably Benign.
2 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 38 of 38] 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 105183 APN Abca12 1.000 IGL01723 G1 1 71314168 A705V G A missense Het probably benign 0.015 phenotype 01/21/2014
2 105184 APN Abcc10 0.089 IGL01723 G1 17 46313745 C728S A T missense Het probably damaging 1.000 phenotype 01/21/2014
3 278801 APN Alms1 0.000 IGL01723 G1 6 85628094 R1773Q G A missense Het probably benign 0.014 phenotype 04/16/2015
4 105170 APN BC067074 0.292 IGL01723 G1 13 113367557 Q198L A T missense Het possibly damaging 0.911 01/21/2014
5 105185 APN C030048H21Rik IGL01723 G1 2 26254768 S1316P A G missense Het possibly damaging 0.827 01/21/2014
6 105178 APN Cd86 0.085 IGL01723 G1 16 36607124 L281S A G missense Het probably benign 0.000 phenotype 01/21/2014
7 105167 APN Cdon 0.486 IGL01723 G1 9 35503338 P1170S C T missense Het probably benign 0.055 phenotype 01/21/2014
8 105191 APN Col11a2 0.930 IGL01723 G1 17 34061280 T A unclassified Het probably benign phenotype 01/21/2014
9 105176 APN Cyp2j12 0.091 IGL01723 G1 4 96102126 V401A A G missense Het possibly damaging 0.564 01/21/2014
10 105166 APN Cyp7a1 0.288 IGL01723 G1 4 6272442 I257N A T missense Het probably damaging 1.000 phenotype 01/21/2014
11 105168 APN Ddhd2 0.167 IGL01723 G1 8 25735011 L593* A T nonsense Het probably null phenotype 01/21/2014
12 105188 APN Dnah8 0.300 IGL01723 G1 17 30708471 L1367S T C missense Het probably damaging 1.000 phenotype 01/21/2014
13 105187 APN Dsg4 0.733 IGL01723 G1 18 20466510 V728M G A missense Het probably damaging 0.997 phenotype 01/21/2014
14 105180 APN Dsp 1.000 IGL01723 G1 13 38179084 V447M G A missense Het probably damaging 1.000 phenotype 01/21/2014
15 105182 APN Epx 0.082 IGL01723 G1 11 87869402 R462H C T missense Het probably damaging 0.999 phenotype 01/21/2014
16 105186 APN Fgf18 1.000 IGL01723 G1 11 33134332 T41A T C missense Het probably damaging 1.000 phenotype 01/21/2014
17 105169 APN Fh1 1.000 IGL01723 G1 1 175601542 A469D G T missense Het probably damaging 1.000 phenotype 01/21/2014
18 105162 APN Hcn1 0.000 IGL01723 G1 13 117976055 S852R A C missense Het probably damaging 0.975 phenotype 01/21/2014
19 105181 APN Hmcn1 0.000 IGL01723 G1 1 150744960 S1166R A T missense Het probably benign 0.008 phenotype 01/21/2014
20 105164 APN Krt78 0.083 IGL01723 G1 15 101951798 G228S C T missense Het possibly damaging 0.653 phenotype 01/21/2014
21 105174 APN Lrrn4 0.089 IGL01723 G1 2 132870061 E614G T C missense Het possibly damaging 0.793 phenotype 01/21/2014
22 105177 APN Mettl9 0.135 IGL01723 G1 7 121052269 I180T T C missense Het possibly damaging 0.665 01/21/2014
23 105175 APN Mgat2 0.672 IGL01723 G1 12 69185641 T330A A G missense Het probably damaging 0.989 phenotype 01/21/2014
24 105192 APN Myh13 0.164 IGL01723 G1 11 67369219 T C unclassified Het probably benign 01/21/2014
25 105172 APN Nipbl 0.968 IGL01723 G1 15 8335071 T1283I G A missense Het possibly damaging 0.711 phenotype 01/21/2014
26 105179 APN Nxpe4 0.112 IGL01723 G1 9 48398598 D387G A G missense Het probably benign 0.002 01/21/2014
27 105165 APN Olfr1110 0.083 IGL01723 G1 2 87135478 V281A A G missense Het probably benign 0.014 phenotype 01/21/2014
28 105161 APN Olfr382 0.203 IGL01723 G1 11 73516626 D191V T A missense Het probably damaging 0.998 phenotype 01/21/2014
29 278802 APN Pcdhb5 0.125 IGL01723 G1 18 37321022 S152A T G missense Het probably benign 0.000 phenotype 04/16/2015
30 105189 APN Pcnt 1.000 IGL01723 G1 10 76418499 R832H C T missense Het possibly damaging 0.629 phenotype 01/21/2014
31 105163 APN Ptprd 0.000 IGL01723 G1 4 76243673 S108R A C missense Het probably damaging 0.996 phenotype 01/21/2014
32 105190 APN Ryr3 0.513 IGL01723 G1 2 112650111 C T critical splice donor site 1 bp Het probably null phenotype 01/21/2014
33 105173 APN Slc22a4 0.481 IGL01723 G1 11 53988845 V463M C T missense Het probably benign 0.279 phenotype 01/21/2014
34 105171 APN Soga1 0.292 IGL01723 G1 2 157030614 M938V T C missense Het probably benign 0.005 01/21/2014
35 278803 APN Ttn 1.000 IGL01723 G1 2 76730404 L29218I A T missense Het probably damaging 0.999 phenotype 04/16/2015
36 278804 APN Ttn 1.000 IGL01723 G1 2 76730402 L29218F T A missense Het probably damaging 1.000 phenotype 04/16/2015
37 105159 APN Vmn2r44 IGL01723 G1 7 8377916 H326L T A missense Het probably damaging 0.968 01/21/2014
38 105160 APN Vps13d 1.000 IGL01723 G1 4 145173145 M188K A T missense Het possibly damaging 0.842 phenotype 01/21/2014
[records 1 to 38 of 38]