Incidental Mutations

14 incidental mutations are currently displayed, and affect 14 genes.
0 are Possibly Damaging.
4 are Probably Damaging.
6 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 14 of 14] 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 8485 APN 4933416C03Rik 0.098 IGL00730 G1 10 116113026 D198E A C missense Het probably benign 0.132 12/06/2012
2 8626 APN Adnp2 1.000 IGL00730 G1 18 80128032 I1054N A T missense Het probably benign 0.000 12/06/2012
3 9382 APN Carf 0.000 IGL00730 G1 1 60147418 Q511* C T nonsense Het probably null phenotype 12/06/2012
4 11228 APN Dnaaf5 0.299 IGL00730 G1 5 139151668 G T critical splice donor site 1 bp Het probably null phenotype 12/06/2012
5 10948 APN Gen1 0.118 IGL00730 G1 12 11261067 N55D T C missense Het probably damaging 0.999 phenotype 12/06/2012
6 11160 APN Gsdmc4 0.062 IGL00730 G1 15 63897804 R190W T A missense Het probably damaging 0.998 12/06/2012
7 11356 APN Hsd3b5 0.070 IGL00730 G1 3 98630057 S48T A T missense Het probably benign 0.048 12/06/2012
8 11708 APN Lactb2 0.061 IGL00730 G1 1 13647516 T G splice site Het probably benign phenotype 12/06/2012
9 277861 APN Mb21d1 0.228 IGL00730 G1 9 78435488 P344L G A missense Het probably damaging 0.988 phenotype 04/16/2015
10 12975 APN Pdzk1 0.182 IGL00730 G1 3 96868426 D370G A G missense Het probably benign 0.000 phenotype 12/06/2012
11 13715 APN Qtrt1 0.439 IGL00730 G1 9 21419549 G T critical splice donor site 1 bp Het probably null phenotype 12/06/2012
12 14502 APN Tmem63c 0.078 IGL00730 G1 12 87077206 L486Q T A missense Het probably benign 0.051 12/06/2012
13 14548 APN Top2b 0.954 IGL00730 G1 14 16389831 Y223C A G missense Het probably damaging 0.995 phenotype 12/06/2012
14 14600 APN Trpm2 0.151 IGL00730 G1 10 77942915 T C splice site 4 bp Het probably null phenotype 12/06/2012
[records 1 to 14 of 14]