Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
4 are Possibly Damaging.
7 are Probably Damaging.
9 are Probably Benign.
4 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 178905 APN 2010111I01Rik 0.085 IGL01876 G1 13 63190522 S570P T C missense Het probably damaging 0.998 phenotype 05/07/2014
2 178912 APN Ap3b2 0.132 IGL01876 G1 7 81473854 T A splice site 3 bp Het probably null phenotype 05/07/2014
3 178913 APN Api5 0.900 IGL01876 G1 2 94418954 A G splice site Het probably benign phenotype 05/07/2014
4 178895 APN Arhgap1 0.382 IGL01876 G1 2 91650219 A G splice site Het probably null phenotype 05/07/2014
5 178907 APN BC003331 0.842 IGL01876 G1 1 150382338 T182N G T missense Het probably benign 0.103 05/07/2014
6 278970 APN C130026I21Rik 0.214 IGL01876 G1 1 85254186 A G intron Het probably benign 04/16/2015
7 178900 APN C330027C09Rik 0.966 IGL01876 G1 16 49001678 V223A T C missense Het probably damaging 0.996 phenotype 05/07/2014
8 178893 APN Cldn6 0.000 IGL01876 G1 17 23681184 V41F G T missense Het probably damaging 0.981 phenotype 05/07/2014
9 178906 APN Dctn1 1.000 IGL01876 G1 6 83197921 V1032L G T missense Het probably damaging 1.000 phenotype 05/07/2014
10 178902 APN Eef2 0.965 IGL01876 G1 10 81180270 F488L T A missense Het probably benign 0.000 phenotype 05/07/2014
11 178897 APN Fars2 1.000 IGL01876 G1 13 36537311 T410A A G missense Het probably benign 0.073 0.124 phenotype 05/07/2014
12 178908 APN Hnrnpc 1.000 IGL01876 G1 14 52081873 N91S T C missense Het probably null 0.011 phenotype 05/07/2014
13 178904 APN Magel2 1.000 IGL01876 G1 7 62378827 V493A T C missense Het possibly damaging 0.678 phenotype 05/07/2014
14 178911 APN Olfr1222 0.079 IGL01876 G1 2 89125737 A T splice site Het probably null phenotype 05/07/2014
15 178894 APN Olfr199 0.060 IGL01876 G1 16 59216019 V198A A G missense Het possibly damaging 0.895 phenotype 05/07/2014
16 178901 APN Pcnx2 0.000 IGL01876 G1 8 125866031 S731R G T missense Het probably benign 0.315 phenotype 05/07/2014
17 178892 APN Plekhm1 0.000 IGL01876 G1 11 103376751 L798P A G missense Het probably damaging 1.000 phenotype 05/07/2014
18 178899 APN Prkd1 1.000 IGL01876 G1 12 50366348 E680G T C missense Het probably damaging 1.000 phenotype 05/07/2014
19 178909 APN Rabggta 0.967 IGL01876 G1 14 55718671 T140A T C missense Het probably damaging 0.980 phenotype 05/07/2014
20 178896 APN Slc2a1 1.000 IGL01876 G1 4 119133378 D236N G A missense Het probably benign 0.114 phenotype 05/07/2014
21 178898 APN Sptlc1 1.000 IGL01876 G1 13 53374012 V39F C A missense Het probably benign 0.017 phenotype 05/07/2014
22 178910 APN Svs1 0.056 IGL01876 G1 6 48990036 R639S A T missense Het possibly damaging 0.711 05/07/2014
23 178891 APN Vmn1r6 0.141 IGL01876 G1 6 57002461 K36R A G missense Het probably benign 0.119 05/07/2014
24 278969 APN Vmn2r-ps159 0.664 IGL01876 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
25 178903 APN Wdpcp 0.666 IGL01876 G1 11 21813383 D581E T A missense Het possibly damaging 0.916 phenotype 05/07/2014
[records 1 to 25 of 25]