Incidental Mutations

8 incidental mutations are currently displayed, and affect 8 genes.
2 are Possibly Damaging.
1 are Probably Damaging.
2 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
1 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 44062 UTSW 2510039O18Rik 0.201 V5088 225 N 521 4 147941776 S251F C T missense Het probably benign 0.184 05/31/2013
2 44067 UTSW Akap8l 0.646 V5088 163 N 521 17 32336739 C G critical splice acceptor site Het probably null 05/31/2013
3 44066 UTSW Ccar2 0.397 V5088 215 N 521 14 70151289 L158I G T missense Het probably damaging 0.988 phenotype 05/31/2013
4 44064 UTSW Megf11 0.251 V5088 149 N 521 9 64690069 C674* C A nonsense Het probably null phenotype 05/31/2013
5 44069 UTSW Olfr136 0.076 V5088 200 N 521 17 38335159 M1V A G start codon destroyed Het probably null 0.991 phenotype 05/31/2013
6 44065 UTSW Psme4 0.000 V5088 225 N 521 11 30851210 E1455G A G missense Het probably benign 0.169 0.186 phenotype 05/31/2013
7 44063 UTSW Wdr17 0.153 V5088 218 N 521 8 54693096 A90T C T missense Het possibly damaging 0.845 0.078 phenotype 05/31/2013
8 44068 UTSW Zbtb12 0.088 V5088 159 N 521 17 34896301 A354E C A missense Het possibly damaging 0.832 0.092 05/31/2013
[records 1 to 8 of 8]