Incidental Mutations

8 incidental mutations are currently displayed, and affect 8 genes.
0 are Possibly Damaging.
4 are Probably Damaging.
2 are Probably Benign.
2 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 8 of 8] 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 76982 UTSW Cdhr2 0.067 R0774 G1 225 N 13 54717855 S222F C T missense Het probably damaging 0.999 phenotype 10/16/2013
2 76979 UTSW Leng8 0.964 R0774 G1 225 N 7 4142136 H178Q T A missense Het probably damaging 0.995 10/16/2013
3 76981 UTSW Prl3b1 0.085 R0774 G1 225 N 13 27243865 A53T G A missense Het probably benign 0.001 0.090 10/16/2013
4 76978 UTSW Psip1 0.521 R0774 G1 217 N 4 83460452 CACTTACT CACT frame shift Het probably null phenotype 10/16/2013
5 76976 UTSW Shox2 1.000 R0774 G1 225 N 3 66973811 A279T C T missense Het probably damaging 0.998 phenotype 10/16/2013
6 76977 UTSW Sis 0.000 R0774 G1 225 N 3 72952531 Q297R T C missense Het probably damaging 1.000 phenotype 10/16/2013
7 76980 UTSW Slc1a6 0.081 R0774 G1 95 N 10 78812824 V460L G T missense Het probably benign 0.030 phenotype 10/16/2013
8 99105 UTSW St5 0.514 R0774 G1 225 N 7 109542320 C T splice site Het probably null phenotype 01/10/2014
[records 1 to 8 of 8]