Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
6 are Possibly Damaging.
4 are Probably Damaging.
17 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 51537 APN 5830411N06Rik 0.000 IGL01101 G1 7 140296104 Q543L A T missense Het probably benign 0.349 06/21/2013
2 52796 APN Adamts20 0.089 IGL01101 G1 15 94344042 D695V T A missense Het probably damaging 1.000 phenotype 06/21/2013
3 53246 APN Ahnak 0.244 IGL01101 G1 19 9012887 T C intron Het probably benign phenotype 06/21/2013
4 53329 APN Akap4 IGL01101 G1 X 7076184 M242K T A missense Het probably benign 0.150 phenotype 06/21/2013
5 51314 APN Cd207 0.051 IGL01101 G1 6 83675857 D97G T C missense Het probably benign 0.253 phenotype 06/21/2013
6 50898 APN Cdc20 1.000 IGL01101 G1 4 118435552 V333A A G missense Het possibly damaging 0.840 phenotype 06/21/2013
7 52566 APN Cdhr2 0.064 IGL01101 G1 13 54718135 A G splice site Het probably benign phenotype 06/21/2013
8 50266 APN Cfhr1 0.070 IGL01101 G1 1 139553584 Y186F T A missense Het probably benign 0.112 phenotype 06/21/2013
9 50897 APN Cnbd1 0.000 IGL01101 G1 4 18907098 I159F T A missense Het probably benign 0.302 06/21/2013
10 50896 APN Cyp2j11 0.070 IGL01101 G1 4 96339095 M228R A C missense Het probably benign 0.000 06/21/2013
11 52678 APN Dach1 1.000 IGL01101 G1 14 97840204 S581I C A missense Het possibly damaging 0.834 phenotype 06/21/2013
12 52298 APN Dbnl 0.185 IGL01101 G1 11 5793722 D71G A G missense Het possibly damaging 0.937 phenotype 06/21/2013
13 53327 APN F8 0.322 IGL01101 G1 X 75287387 T966S T A missense Het possibly damaging 0.623 phenotype 06/21/2013
14 51921 APN Filip1 0.331 IGL01101 G1 9 79898246 L75F T A missense Het probably benign 0.440 phenotype 06/21/2013
15 51538 APN Foxi2 0.000 IGL01101 G1 7 135412007 Y322C A G missense Het probably benign 0.071 phenotype 06/21/2013
16 52296 APN Ftsj3 0.970 IGL01101 G1 11 106255632 V7A A G missense Het probably benign 0.159 phenotype 06/21/2013
17 52677 APN Gm8362 IGL01101 G1 14 6767109 S204T A T missense Het probably benign 0.004 06/21/2013
18 51922 APN Ibtk 0.000 IGL01101 G1 9 85732622 C A splice site Het probably benign phenotype 06/21/2013
19 52921 APN Marf1 0.145 IGL01101 G1 16 14146736 V267I C T missense Het possibly damaging 0.854 phenotype 06/21/2013
20 51920 APN Mmp27 0.077 IGL01101 G1 9 7573415 D169E T A missense Het probably damaging 1.000 phenotype 06/21/2013
21 50510 APN Olfr1115 0.060 IGL01101 G1 2 87252462 T175K C A missense Het probably damaging 0.999 phenotype 06/21/2013
22 50509 APN Olfr1247 0.136 IGL01101 G1 2 89609847 C85Y C T missense Het probably benign 0.005 phenotype 06/21/2013
23 52679 APN Olfr728 0.290 IGL01101 G1 14 50140054 M195K A T missense Het probably benign 0.058 phenotype 06/21/2013
24 52297 APN P4ha2 0.295 IGL01101 G1 11 54119305 C296F G T missense Het probably damaging 1.000 phenotype 06/21/2013
25 53328 APN Slc38a5 IGL01101 G1 X 8271511 T C intron Het probably benign phenotype 06/21/2013
26 51763 APN Sorbs2 0.000 IGL01101 G1 8 45745423 R36L G T missense Het possibly damaging 0.930 phenotype 06/21/2013
27 52920 APN Tmem207 0.053 IGL01101 G1 16 26517877 Y42* A C nonsense Het probably null 06/21/2013
28 278175 APN Vmn2r115 0.115 IGL01101 G1 17 23345997 R286K G A missense Het probably benign 0.116 04/16/2015
[records 1 to 28 of 28]