Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
3 are Possibly Damaging.
9 are Probably Damaging.
9 are Probably Benign.
3 are Probably Null.
1 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 179620 APN 4933402N22Rik IGL01904 G1 5 11921456 N125T A C missense Het probably benign 0.057 05/07/2014
2 179617 APN Dnah5 0.808 IGL01904 G1 15 28307364 I1746T T C missense Het probably benign 0.091 phenotype 05/07/2014
3 179629 APN Eml3 0.774 IGL01904 G1 19 8936766 T C splice site Het probably benign 05/07/2014
4 179624 APN Eml6 0.280 IGL01904 G1 11 29838613 E491* C A nonsense Het probably null 05/07/2014
5 279061 APN Gm10717 0.698 IGL01904 G1 9 3025616 S67L C T missense Het probably benign 0.002 04/16/2015
6 279060 APN Gm10718 0.581 IGL01904 G1 9 3025118 Y194F A T missense Het probably benign 0.001 04/16/2015
7 279059 APN Gm21738 0.795 IGL01904 G1 14 19416979 S144L G A missense Het probably benign 0.011 04/16/2015
8 179621 APN Hs3st2 0.000 IGL01904 G1 7 121500984 P351L C T missense Het probably damaging 1.000 phenotype 05/07/2014
9 179626 APN Igf2r 0.900 IGL01904 G1 17 12714911 Y819N A T missense Het probably damaging 0.994 phenotype 05/07/2014
10 179615 APN Kifc3 0.000 IGL01904 G1 8 95137957 A42S C A missense Het possibly damaging 0.805 phenotype 05/07/2014
11 179627 APN Mrps17 0.252 IGL01904 G1 5 129716801 T20A A G missense Het probably damaging 1.000 phenotype 05/07/2014
12 179625 APN Msh6 1.000 IGL01904 G1 17 87984732 V305A T C missense Het probably benign 0.000 phenotype 05/07/2014
13 179616 APN Olfr449 0.082 IGL01904 G1 6 42838289 M136T T C missense Het possibly damaging 0.759 phenotype 05/07/2014
14 179612 APN Olfr872 0.058 IGL01904 G1 9 20260290 M150R T G missense Het probably damaging 0.992 phenotype 05/07/2014
15 179618 APN Pappa2 0.000 IGL01904 G1 1 158783941 L1484P A G missense Het probably damaging 0.986 phenotype 05/07/2014
16 179630 APN Polr3c 0.960 IGL01904 G1 3 96716665 A T critical splice donor site 2 bp Het probably null 05/07/2014
17 179623 APN Ros1 0.180 IGL01904 G1 10 52077911 E1877D C A missense Het probably damaging 0.974 phenotype 05/07/2014
18 179619 APN Slc5a4b 0.188 IGL01904 G1 10 76060426 N565S T C missense Het probably damaging 0.977 05/07/2014
19 179628 APN Slf2 0.903 IGL01904 G1 19 44949141 T C critical splice donor site 2 bp Het probably null 05/07/2014
20 179632 APN Suclg2 0.000 IGL01904 G1 6 95588934 A T splice site Het probably benign phenotype 05/07/2014
21 179622 APN Sult2a8 0.063 IGL01904 G1 7 14425457 E79G T C missense Het probably damaging 1.000 05/07/2014
22 179614 APN Triobp 1.000 IGL01904 G1 15 78967364 T573A A G missense Het possibly damaging 0.795 phenotype 05/07/2014
23 279062 APN Vmn2r-ps159 0.678 IGL01904 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
24 179631 APN Zfand5 0.786 IGL01904 G1 19 21279758 C T unclassified Het probably benign phenotype 05/07/2014
25 179613 APN Zfhx4 0.786 IGL01904 G1 3 5412709 H3461Q C A missense Het probably damaging 0.998 05/07/2014
[records 1 to 25 of 25]