Incidental Mutations

23 incidental mutations are currently displayed, and affect 23 genes.
1 are Possibly Damaging.
7 are Probably Damaging.
10 are Probably Benign.
4 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 23 of 23] 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 12464 APN Ap4e1 0.190 IGL00659 G1 2 127063301 V964A T C missense Het probably benign 0.301 phenotype 12/06/2012
2 12497 APN Birc6 1.000 IGL00659 G1 17 74660653 V4197E T A missense Het probably damaging 1.000 phenotype 12/06/2012
3 12500 APN C8b 0.000 IGL00659 G1 4 104801334 T A splice site Het probably benign phenotype 12/06/2012
4 12523 APN Cdh13 0.000 IGL00659 G1 8 119312667 D616G A G missense Het probably damaging 0.997 phenotype 12/06/2012
5 12533 APN Cfi 0.000 IGL00659 G1 3 129836813 K2E A G missense Het unknown phenotype 12/06/2012
6 12534 APN Chek1 1.000 IGL00659 G1 9 36722599 C A splice site 5 bp Het probably null phenotype 12/06/2012
7 28287 APN Chst11 1.000 IGL00659 G1 10 83191805 T G utr 3 prime Het probably benign phenotype 04/17/2013
8 12576 APN Dhx29 1.000 IGL00659 G1 13 112966635 A G splice site Het probably benign phenotype 12/06/2012
9 12605 APN Erbb3 1.000 IGL00659 G1 10 128570983 S1049P A G missense Het probably damaging 0.990 phenotype 12/06/2012
10 12622 APN Fkbp15 0.000 IGL00659 G1 4 62333680 T C splice site Het probably benign 12/06/2012
11 12625 APN Fxr2 0.611 IGL00659 G1 11 69640250 Q51K C A missense Het probably benign 0.115 phenotype 12/06/2012
12 12701 APN Kpna7 0.390 IGL00659 G1 5 145007246 I50F T A missense Het probably damaging 0.999 phenotype 12/06/2012
13 12725 APN Mdm2 1.000 IGL00659 G1 10 117702299 R65G T C missense Het possibly damaging 0.914 phenotype 12/06/2012
14 12749 APN N4bp1 0.000 IGL00659 G1 8 86861802 D169E G T missense Het probably damaging 1.000 12/06/2012
15 12755 APN Nlrp9a 0.068 IGL00659 G1 7 26557625 I134V A G missense Het probably benign 0.220 12/06/2012
16 13063 APN Plrg1 1.000 IGL00659 G1 3 83070673 S400T T A missense Het probably damaging 0.993 phenotype 12/06/2012
17 13089 APN Polr1b 1.000 IGL00659 G1 2 129118100 T C critical splice donor site 2 bp Het probably null phenotype 12/06/2012
18 13950 APN Sec23b 1.000 IGL00659 G1 2 144583770 T C critical splice donor site 2 bp Het probably null phenotype 12/06/2012
19 14689 APN Ubr4 1.000 IGL00659 G1 4 139421245 T1680I C T missense Het probably damaging 1.000 phenotype 12/06/2012
20 14740 APN Usp29 0.000 IGL00659 G1 7 6962282 N375D A G missense Het probably benign 0.061 12/06/2012
21 14873 APN Wrn 0.592 IGL00659 G1 8 33322377 A G splice site Het probably benign phenotype 12/06/2012
22 14973 APN Zfp422 0.000 IGL00659 G1 6 116626505 Q178* G A nonsense Het probably null phenotype 12/06/2012
23 15014 APN Zfp938 0.077 IGL00659 G1 10 82227521 T A utr 3 prime Het probably benign 12/06/2012
[records 1 to 23 of 23]