Variant #0000000071 (NC_000007.13:g.117234995T>G, NM_000492.3:c.2502T>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.117234995T>G
Reference -
DB-ID CFTR_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00029 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2019-02-21 11:13:15 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 ?/? 15 c.2502T>G r.(?) p.(Phe834Leu)