chr7:117592008:A>G Detail (hg38) (CFTR)

Information

Genome

Assembly Position
hg19 chr7:117,232,062-117,232,062 View the variant detail on this assembly version.
hg38 chr7:117,592,008-117,592,008

HGVS

Type Transcript Protein
RefSeq NM_000492.3:c.1841A>G NP_000483.3:p.Asp614Gly
Ensemble ENST00000003084.11:c.1841A>G ENST00000003084.11:p.Asp614Gly
ENST00000648260.1:c.1402-10818A>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Pathogenic Likely pathogenic
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 tgv351814552 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic Likely pathogenic 2023-10-11 criteria provided, multiple submitters, no conflicts cystic fibrosis germline unknown Detail
Pathogenic criteria provided, single submitter Congenital bilateral aplasia of vas deferens from CFTR mutation,cystic fibrosis germline Detail
Pathogenic criteria provided, single submitter Congenital bilateral aplasia of vas deferens from CFTR mutation,cystic fibrosis germline Detail
Pathogenic 2015-07-03 criteria provided, single submitter CFTR-related disorder,cystic fibrosis germline Detail
Pathogenic 2015-07-03 criteria provided, single submitter CFTR-related disorder,cystic fibrosis germline Detail
Likely pathogenic 2022-10-12 criteria provided, single submitter CFTR-related disorder germline Detail
Pathogenic 2023-10-02 criteria provided, multiple submitters, no conflicts not provided germline unknown Detail
Pathogenic 2023-10-31 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
Annotation

Annotations

DescrptionSourceLinks
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND Cystic fibrosis ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND multiple conditions ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND multiple conditions ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND multiple conditions ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND multiple conditions ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND CFTR-related disorder ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND not provided ClinVar Detail
NM_000492.4(CFTR):c.1841A>G (p.Asp614Gly) AND Bronchiectasis with or without elevated sweat chloride... ClinVar Detail
NA 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
rs201124247 dbSNP
Genome
hg38
Position
chr7:117,592,008-117,592,008
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Heterozygous Counts in All Race (ExAC)
3
Homozygous Counts in All Race (ExAC)
0
East Asian Chromosome Counts (ExAC)
8642
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
119098
Allele Counts in All Race (ExAC)
3
Allele Frequency in All Race (ExAC)
2.5189339871366438E-5
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