Incidental Mutations

11 incidental mutations are currently displayed, and affect 11 genes.
1 are Possibly Damaging.
4 are Probably Damaging.
6 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 11 of 11] 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 8445 APN 2900092C05Rik 0.052 IGL00714 G1 7 12556004 A C splice site Het probably benign 12/06/2012
2 9403 APN Casp8ap2 1.000 IGL00714 G1 4 32649192 Q1951R A G missense Het probably damaging 0.997 phenotype 12/06/2012
3 9492 APN Cd22 0.000 IGL00714 G1 7 30876147 M157V T C missense Het probably benign 0.006 phenotype 12/06/2012
4 9918 APN Csta1 0.056 IGL00714 G1 16 36124999 V48A A G missense Het probably damaging 0.999 12/06/2012
5 10850 APN Fxr1 1.000 IGL00714 G1 3 34047627 T C splice site Het probably benign phenotype 12/06/2012
6 12923 APN Pcdh1 0.417 IGL00714 G1 18 38198729 T407I G A missense Het possibly damaging 0.655 phenotype 12/06/2012
7 12929 APN Pcdha1 0.000 IGL00714 G1 18 36932175 T631S A T missense Het probably damaging 0.992 phenotype 12/06/2012
8 13949 APN Sec23b 1.000 IGL00714 G1 2 144559225 A2V C T missense Het probably benign 0.334 phenotype 12/06/2012
9 14381 APN Tbc1d2 0.168 IGL00714 G1 4 46649745 V97A A G missense Het probably benign 0.037 12/06/2012
10 14645 APN Ttll9 0.067 IGL00714 G1 2 152984260 E130A A C missense Het probably damaging 0.994 12/06/2012
11 14947 APN Zfp160 0.000 IGL00714 G1 17 21026702 T505S A T missense Het probably benign 0.000 12/06/2012
[records 1 to 11 of 11]