Variant #0000219715 (NC_000002.11:g.31754565T>C, NC_000002.11(NM_000348.3):c.547-38A>G (SRD5A2))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.31754565T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SRD5A2_000026
Frequency 1/12176
Freq. EA 1/8280
Freq. AA 0/3896
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-03 22:04:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SRD5A2 NM_000348.3 ?/? c.547-38A>G r.(=) p.(=)