Variant #0001043398 (NC_000011.9:g.193953C>A, NC_000011.9(NM_145651.2):c.255+42C>A (SCGB1C1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.193953C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SCGB1C1_000033
Frequency 1/12820
Freq. EA 1/8510
Freq. AA 0/4310
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 2014-05-04 00:00:58 +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.255+42C>A r.(=) p.(=)