Variant #0000712180 (NC_000007.13:g.117174411T>G, NM_000492.3:c.571T>G (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.117174411T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CFTR_001320 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs141482808
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-01-19 11:55:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 +/. - c.571T>G r.(?) p.(Phe191Val)


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