Incidental Mutations

6 incidental mutations are currently displayed, and affect 6 genes.
0 are Possibly Damaging.
1 are Probably Damaging.
3 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 6 of 6] 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 69481 UTSW 4921517D22Rik 0.057 R0757 G1 217 N 13 59691598 GCC GC frame shift Het probably null 0.646 09/30/2013
2 69480 UTSW Muc6 0.496 R0757 G1 96 N 7 141638584 S2059A A C missense Het probably benign 0.061 phenotype 09/30/2013
3 69479 UTSW Plppr5 0.234 R0757 G1 225 N 3 117575891 V66M G A missense Het probably benign 0.164 phenotype 09/30/2013
4 69482 UTSW Psmg2 0.912 R0757 G1 217 N 18 67646025 CTTCAGTT CTTCAGTTCAGTT frame shift Het probably null 09/30/2013
5 99017 UTSW Scrib 1.000 R0757 G1 111 N 15 76062750 TCTCCTCCTCCTCCTCCTC TCTCCTCCTCCTCCTC small deletion Het probably benign phenotype 01/10/2014
6 69483 UTSW Tll2 0.804 R0757 G1 225 N 19 41120228 R328C G A missense Het probably damaging 1.000 0.434 phenotype 09/30/2013
[records 1 to 6 of 6]