Incidental Mutations

24 incidental mutations are currently displayed, and affect 24 genes.
3 are Possibly Damaging.
9 are Probably Damaging.
6 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 24 of 24] 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 181660 APN Ahr 0.951 IGL01972 G1 12 35504449 D557A T G missense Het possibly damaging 0.889 phenotype 05/07/2014
2 181661 APN Akap11 0.000 IGL01972 G1 14 78507857 Q1697R T C missense Het probably damaging 0.993 phenotype 05/07/2014
3 181659 APN Alpi 0.102 IGL01972 G1 1 87099709 T312S T A missense Het probably damaging 0.998 phenotype 05/07/2014
4 181670 APN Cacna1b 0.000 IGL01972 G1 2 24635095 C A critical splice donor site 1 bp Het probably null phenotype 05/07/2014
5 181668 APN Car5a 0.124 IGL01972 G1 8 121927082 C T critical splice donor site 1 bp Het probably null phenotype 05/07/2014
6 181650 APN Cubn 1.000 IGL01972 G1 2 13446072 T841A T C missense Het possibly damaging 0.899 phenotype 05/07/2014
7 181664 APN Eml6 0.250 IGL01972 G1 11 29838451 F545I A T missense Het possibly damaging 0.669 05/07/2014
8 181651 APN Fam114a2 0.138 IGL01972 G1 11 57509394 T156I G A missense Het probably damaging 0.999 05/07/2014
9 181666 APN Fam160a2 0.000 IGL01972 G1 7 105390145 N5S T C missense Het probably damaging 0.989 phenotype 05/07/2014
10 181652 APN Fbxl21 0.000 IGL01972 G1 13 56536859 R259* C T nonsense Het probably null phenotype 05/07/2014
11 181648 APN Gm5117 0.880 IGL01972 G1 8 31737759 C T exon Het noncoding transcript 05/07/2014
12 181662 APN Hc 0.573 IGL01972 G1 2 34983772 Y1650C T C missense Het probably damaging 0.998 phenotype 05/07/2014
13 181663 APN Med12l 0.315 IGL01972 G1 3 59261893 T1568K C A missense Het probably damaging 0.996 phenotype 05/07/2014
14 181657 APN Olfr429 0.080 IGL01972 G1 1 174089421 C127F G T missense Het probably damaging 0.994 phenotype 05/07/2014
15 181656 APN Olfr701 0.087 IGL01972 G1 7 106818532 I150V A G missense Het probably benign 0.014 phenotype 05/07/2014
16 181647 APN Olfr996 0.094 IGL01972 G1 2 85579773 F178S T C missense Het probably damaging 0.997 phenotype 05/07/2014
17 181667 APN Orm3 0.051 IGL01972 G1 4 63359326 S184G A G missense Het probably benign 0.000 05/07/2014
18 181669 APN Padi1 0.110 IGL01972 G1 4 140818859 A G splice site Het probably benign phenotype 05/07/2014
19 181658 APN Rnf133 0.095 IGL01972 G1 6 23648989 T357A T C missense Het probably benign 0.001 phenotype 05/07/2014
20 181653 APN Skiv2l2 0.961 IGL01972 G1 13 112881061 K853E T C missense Het probably damaging 0.996 05/07/2014
21 181654 APN Tmem17 0.201 IGL01972 G1 11 22517265 S60G A G missense Het probably benign 0.005 05/07/2014
22 181655 APN Ubqlnl 0.110 IGL01972 G1 7 104149697 Q198K G T missense Het probably benign 0.002 phenotype 05/07/2014
23 181649 APN Vmn1r69 0.069 IGL01972 G1 7 10580659 Y48* A T nonsense Het probably null 05/07/2014
24 181665 APN Zfp658 0.000 IGL01972 G1 7 43572710 W136* G A nonsense Het probably null 05/07/2014
[records 1 to 24 of 24]