Variant #0001043381 (NC_000011.9:g.193703G>A, NC_000011.9(NM_145651.2):c.56-9G>A (SCGB1C1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.193703G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SCGB1C1_000016
Frequency 5/12692
Freq. EA 5/8454
Freq. AA 0/4238
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 16:37:25 +02:00 (CEST)
Date last edited 2014-04-28 04:51:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SCGB1C1 NM_145651.2 ?/? c.56-9G>A r.(=) p.(=)