Variant #0001465079 (NC_000016.9:g.12059278C>T, NM_001192.2:c.97C>T (TNFRSF17))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.12059278C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TNFRSF17_000007
Frequency 2/12994
Freq. EA 2/8600
Freq. AA 0/4394
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 12:41:17 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF17 NM_001192.2 ?/? c.97C>T r.(?) p.(Pro33Ser)