Variant #0001043396 (NC_000011.9:g.193925G>A, NC_000011.9(NM_145651.2):c.255+14G>A (SCGB1C1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.193925G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SCGB1C1_000031
Frequency 1289/12814
Freq. EA 902/8522
Freq. AA 387/4292
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 17:40:25 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SCGB1C1 NM_145651.2 ?/? c.255+14G>A r.(=) p.(=)