Variant #0000000134 (NC_000007.13:g.117267812T>G, NM_000492.3:c.3705T>G (CFTR))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.117267812T>G
Reference -
DB-ID CFTR_000004
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00492 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-16 10:51:12 +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 ?/? 8 c.3705T>G r.(?) p.(Ser1235Arg)