Variant #0001208177 (NC_000012.11:g.53715116G>C, NC_000012.11(NM_001173466.1):c.123+11C>G (AAAS))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.53715116G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAAS_000116
Frequency 1/13004
Freq. EA 0/8600
Freq. AA 1/4404
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 16:39:18 +02:00 (CEST)
Date last edited 2018-08-23 01:20:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAAS NM_001173466.1 ?/? c.123+11C>G r.(=) p.(=)