Variant #0000880225 (NC_000009.11:g.135049_135050insTG, NC_000009.11(NM_018491.3):c.765-20_765-19insCA (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.135049_135050insTG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000016
Frequency 8/2316
Freq. EA 7/1520
Freq. AA 1/796
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 16:29:58 +02:00 (CEST)
Date last edited 2020-08-30 01:14:01 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CBWD1 NM_018491.3 ?/? c.765-20_765-19insCA r.(=) p.(=)