Variant #0000000106 (NC_000007.13:g.117230411G>C, NM_000492.3:c.1684G>C (CFTR))

Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.117230411G>C
Reference -
DB-ID CFTR_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2020-10-08 09:08:07 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 ./? 13 c.1684G>C r.(?) p.(Val562Leu)