Incidental Mutations

5 incidental mutations are currently displayed, and affect 5 genes.
0 are Possibly Damaging.
1 are Probably Damaging.
2 are Probably Benign.
2 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 5 of 5] 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?
 
1 573 UTSW C2cd5 0.389 D605 G1 Y 6 143029660 V787I C T missense Het probably benign 0.001 0.086 11/24/2010
2 570 UTSW Kat2b 0.000 D605 G1 Y 17 53629330 R99G A G missense Het probably damaging 1.000 0.832 phenotype 11/24/2010
3 572 UTSW Ly75 0.000 D605 G1 Y 2 60352352 A G critical splice donor site 2 bp Het probably null 0.958 phenotype 11/29/2010
4 571 UTSW Olfr1474 0.063 D605 G1 Y 19 13471157 C62* T A nonsense Het probably null 0.976 phenotype 11/24/2010
5 574 UTSW Sfmbt2 1.000 D605 G1 Y 2 10579325 T864I C T missense Het probably benign 0.079 0.090 11/29/2010
[records 1 to 5 of 5]