Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
5 are Possibly Damaging.
14 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 34 of 34] 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 362844 APN Abcg4 0.174 IGL02882 9 44277489 L469* A T nonsense Het probably null phenotype 12/18/2015
2 362847 APN Calr3 0.128 IGL02882 8 72434821 Y46F T A missense Het probably damaging 0.994 phenotype 12/18/2015
3 362842 APN Clcn4 0.000 IGL02882 7 7290465 C491R A G missense Het probably damaging 1.000 phenotype 12/18/2015
4 362833 APN Col6a5 0.864 IGL02882 9 105934321 D666E G T missense Het unknown phenotype 12/18/2015
5 362826 APN D130052B06Rik 0.125 IGL02882 11 33623780 V126M G A missense Het probably damaging 0.988 12/18/2015
6 362837 APN Ddx27 0.964 IGL02882 2 167027913 I389M A G missense Het possibly damaging 0.862 phenotype 12/18/2015
7 362831 APN Dgka 0.297 IGL02882 10 128733384 I160V T C missense Het possibly damaging 0.771 phenotype 12/18/2015
8 362829 APN E430018J23Rik 0.078 IGL02882 7 127392252 Y188H A G missense Het probably damaging 1.000 12/18/2015
9 362836 APN Enpp6 0.161 IGL02882 8 47030532 S120P T C missense Het probably damaging 0.995 phenotype 12/18/2015
10 362853 APN Ezh1 0.000 IGL02882 11 101203289 I459T A G missense Het probably benign 0.020 phenotype 12/18/2015
11 362857 APN Fam91a1 0.000 IGL02882 15 58453061 A G splice site Het probably benign phenotype 12/18/2015
12 362835 APN Foxn2 0.236 IGL02882 17 88462947 L74P T C missense Het probably damaging 0.999 phenotype 12/18/2015
13 362849 APN Fscn2 0.136 IGL02882 11 120362499 V264A T C missense Het probably benign 0.000 phenotype 12/18/2015
14 362850 APN Gmeb2 0.188 IGL02882 2 181265883 T54I G A missense Het probably damaging 0.980 phenotype 12/18/2015
15 362828 APN Hmcn2 0.000 IGL02882 2 31413367 K3007* A T nonsense Het probably null 12/18/2015
16 362858 APN Ice1 0.939 IGL02882 13 70624474 A T splice site Het probably benign 12/18/2015
17 362832 APN Lgi1 0.774 IGL02882 19 38284005 D84G A G missense Het probably benign 0.238 phenotype 12/18/2015
18 362845 APN Mier2 0.192 IGL02882 10 79547721 I196V T C missense Het probably damaging 0.998 12/18/2015
19 362851 APN Nipal2 0.057 IGL02882 15 34600077 Y198C T C missense Het probably damaging 1.000 12/18/2015
20 362841 APN Npas2 0.000 IGL02882 1 39312996 S176R A C missense Het probably benign 0.075 phenotype 12/18/2015
21 362830 APN Olfr914 0.063 IGL02882 9 38606938 I158F A T missense Het probably benign 0.042 0.090 phenotype 12/18/2015
22 362852 APN Pam 1.000 IGL02882 1 97840367 C713G A C missense Het probably damaging 1.000 phenotype 12/18/2015
23 362854 APN Pcdh17 0.137 IGL02882 14 84446661 D189E C A missense Het probably damaging 0.981 phenotype 12/18/2015
24 362834 APN Pcdhb8 0.067 IGL02882 18 37356223 I318N T A missense Het possibly damaging 0.949 12/18/2015
25 362838 APN Pcyt2 1.000 IGL02882 11 120611407 S300P A G missense Het possibly damaging 0.947 phenotype 12/18/2015
26 362843 APN Pkdrej 0.076 IGL02882 15 85817296 S1480P A G missense Het probably damaging 1.000 phenotype 12/18/2015
27 362859 APN Plekhd1 0.059 IGL02882 12 80719007 G A critical splice donor site 1 bp Het probably null 12/18/2015
28 362839 APN Plxna2 0.000 IGL02882 1 194762570 S757C A T missense Het probably damaging 0.996 phenotype 12/18/2015
29 362856 APN Prkdc 0.951 IGL02882 16 15651519 K163* A T nonsense Het probably null phenotype 12/18/2015
30 362827 APN Serpina3f 0.061 IGL02882 12 104217004 T42S A T missense Het probably damaging 0.998 12/18/2015
31 362840 APN Sesn2 0.272 IGL02882 4 132493793 N456D T C missense Het probably benign 0.161 phenotype 12/18/2015
32 362846 APN Tas2r105 0.055 IGL02882 6 131687180 L95Q A T missense Het possibly damaging 0.948 phenotype 12/18/2015
33 362855 APN Tln1 1.000 IGL02882 4 43539522 V1600A A G missense Het probably benign 0.448 phenotype 12/18/2015
34 362848 APN Zfp808 0.074 IGL02882 13 62173180 K741R A G missense Het probably benign 0.003 12/18/2015
[records 1 to 34 of 34]