chr7:117587805:G>A Detail (hg38) (CFTR, LOC111674475)

Information

Genome

Assembly Position
hg19 chr7:117,227,859-117,227,859 View the variant detail on this assembly version.
hg38 chr7:117,587,805-117,587,805

HGVS

Type Transcript Protein
RefSeq NM_000492.3:c.1651G>A NP_000483.3:p.Gly551Ser
Ensemble ENST00000003084.11:c.1651G>A ENST00000003084.11:p.Gly551Ser
ENST00000648260.1:c.1402-15021G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic; drug response
Review star
Show details
Links
Type Database ID Link
Gene MIM 602421 OMIM
HGNC 1884 HGNC
Ensembl ENSG00000001626 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2017-03-17 reviewed by expert panel cystic fibrosis germline unknown Detail
drug response 2021-03-24 reviewed by expert panel germline Detail
Pathogenic 2020-12-28 criteria provided, multiple submitters, no conflicts not provided germline Detail
Pathogenic 2017-08-28 no assertion criteria provided CFTR-related disorder germline Detail
Pathogenic 2022-05-04 criteria provided, single submitter Hereditary pancreatitis germline Detail
Pathogenic 2023-02-01 criteria provided, single submitter Bronchiectasis with or without elevated sweat chloride 1 unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.800 cystic fibrosis NA CLINVAR Detail
0.800 cystic fibrosis Because PPi stimulated wild-type channels, we tested its effect on CFTR containi... BeFree 7544788 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000492.4(CFTR):c.1651G>A (p.Gly551Ser) AND Cystic fibrosis ClinVar Detail
NM_000492.4(CFTR):c.1651G>A (p.Gly551Ser) AND ivacaftor response - Efficacy ClinVar Detail
NM_000492.4(CFTR):c.1651G>A (p.Gly551Ser) AND not provided ClinVar Detail
NM_000492.4(CFTR):c.1651G>A (p.Gly551Ser) AND CFTR-related disorder ClinVar Detail
NM_000492.4(CFTR):c.1651G>A (p.Gly551Ser) AND Hereditary pancreatitis ClinVar Detail
NM_000492.4(CFTR):c.1651G>A (p.Gly551Ser) AND Bronchiectasis with or without elevated sweat chloride... ClinVar Detail
NA DisGeNET Detail
Because PPi stimulated wild-type channels, we tested its effect on CFTR containing the cystic fibros... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs121909013 dbSNP
Genome
hg38
Position
chr7:117,587,805-117,587,805
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser