Variant #0001070481 (NC_000007.13:g.117120525A>G, NC_000007.13(NM_000492.3):c.53+324A>G (CFTR))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.117120525A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CFTR_001801
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs78171410
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-11 14:43:02 +01:00 (CET)
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.53+324A>G r.(?) p.(?)


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