Variant #0000880402 (NC_000007.13:g.117171092_117171094dup, NM_000492.3:c.413_415dup (CFTR))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.117171092_117171094dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID CFTR_001527 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397508686
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 2022-10-07 11:36:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 +/. - c.413_415dup r.(?) p.(Leu138dup)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.