Variant #0001043366 (NC_000011.9:g.193096T>C, NM_145651.2:c.-4T>C (SCGB1C1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.193096T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SCGB1C1_000001
Frequency 6093/12800
Freq. EA 4199/8524
Freq. AA 1894/4276
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 2014-05-02 14:30:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SCGB1C1 NM_145651.2 ?/? c.-4T>C r.(=) p.(=)