Variant #0001043369 (NC_000011.9:g.193117C>A, NM_145651.2:c.18C>A (SCGB1C1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.193117C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SCGB1C1_000004
Frequency 1/12798
Freq. EA 1/8514
Freq. AA 0/4284
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 2014-05-03 18:45:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SCGB1C1 NM_145651.2 ?/? c.18C>A r.(=) p.(=)