Variant #0000069042 (NC_000001.10:g.47735261A>C, NC_000001.10(NM_003035.2):c.2615+46T>G (STIL))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.47735261A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STIL_000027
Frequency 11/12980
Freq. EA 0/8590
Freq. AA 11/4390
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 18:34:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
STIL NM_003035.2 ?/? c.2615+46T>G r.(=) p.(=)