Variant #0001047713 (NC_000007.13:g.117144344C>T, NM_000492.3:c.91C>T (CFTR))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.117144344C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CFTR_000125 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1800073
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00165 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-05 16:08:01 +02:00 (CEST)
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 -/. - c.91C>T r.(?) p.(Arg31Cys)


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