Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
3 are Possibly Damaging.
12 are Probably Damaging.
7 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
2 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 90763 APN Adamts19 0.000 IGL01557 G1 18 58968720 T A splice site Het probably null phenotype 12/09/2013
2 90762 APN Arl9 0.000 IGL01557 G1 5 77004101 T G critical splice donor site 2 bp Het probably null phenotype 12/09/2013
3 90748 APN Ces3a 0.061 IGL01557 G1 8 105057751 T439K C A missense Het probably damaging 1.000 12/09/2013
4 90750 APN Cyp3a25 0.101 IGL01557 G1 5 145984901 W408R A G missense Het probably damaging 1.000 12/09/2013
5 90742 APN Defb22 0.000 IGL01557 G1 2 152486079 D62A T G missense Het possibly damaging 0.930 12/09/2013
6 90751 APN Dnah17 0.000 IGL01557 G1 11 118073686 R2422Q C T missense Het probably damaging 0.982 phenotype 12/09/2013
7 90760 APN Ehd3 0.000 IGL01557 G1 17 73805280 K13R A G missense Het probably benign 0.000 phenotype 12/09/2013
8 90754 APN Fndc1 0.073 IGL01557 G1 17 7756389 E1406G T C missense Het probably damaging 0.993 12/09/2013
9 90759 APN Gak 1.000 IGL01557 G1 5 108584337 Y762D A C missense Het probably damaging 1.000 phenotype 12/09/2013
10 90756 APN Igf2r 0.920 IGL01557 G1 17 12704635 S1187P A G missense Het possibly damaging 0.822 phenotype 12/09/2013
11 90753 APN Ighmbp2 1.000 IGL01557 G1 19 3281472 E68G T C missense Het probably benign 0.133 phenotype 12/09/2013
12 90752 APN Itpr2 0.000 IGL01557 G1 6 146158976 T2448A T C missense Het probably damaging 0.993 phenotype 12/09/2013
13 90746 APN Lrrk2 0.446 IGL01557 G1 15 91699989 C317W T G missense Het probably damaging 0.998 phenotype 12/09/2013
14 90758 APN Morc1 0.329 IGL01557 G1 16 48498766 S278T T A missense Het probably damaging 0.999 phenotype 12/09/2013
15 90743 APN Mrps9 0.933 IGL01557 G1 1 42851350 V20A T C missense Het probably benign 0.000 phenotype 12/09/2013
16 90757 APN Nutm1 0.000 IGL01557 G1 2 112251818 N304K A T missense Het probably benign 0.363 12/09/2013
17 90741 APN Olfr761 0.137 IGL01557 G1 17 37952851 P58S G A missense Het probably damaging 1.000 phenotype 12/09/2013
18 90745 APN Pcdhb9 0.069 IGL01557 G1 18 37403047 V698A T C missense Het probably damaging 0.998 12/09/2013
19 90747 APN Pitrm1 1.000 IGL01557 G1 13 6552684 D70E C A missense Het probably benign 0.366 phenotype 12/09/2013
20 90749 APN Pkhd1 0.131 IGL01557 G1 1 20116979 T3702A T C missense Het possibly damaging 0.587 phenotype 12/09/2013
21 90764 APN Ppm1h 0.068 IGL01557 G1 10 122782181 A T critical splice acceptor site Het probably null 12/09/2013
22 278576 APN Psmg2 0.959 IGL01557 G1 18 67653223 V218I G A missense Het probably benign 0.000 04/16/2015
23 90744 APN Ptpn5 0.000 IGL01557 G1 7 47081888 Y411C T C missense Het probably damaging 1.000 phenotype 12/09/2013
24 90755 APN Spon2 0.405 IGL01557 G1 5 33216703 A112V G A missense Het probably damaging 1.000 phenotype 12/09/2013
25 90761 APN Zfp648 0.075 IGL01557 G1 1 154204680 V195D T A missense Het probably benign 0.000 12/09/2013
[records 1 to 25 of 25]