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 |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2017-03-17 | reviewed by expert panel | cystic fibrosis |
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Detail |
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2021-03-24 | reviewed by expert panel |
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2020-12-28 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2017-08-28 | no assertion criteria provided | CFTR-related disorder |
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2022-05-04 | criteria provided, single submitter | Hereditary pancreatitis |
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Detail |
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2023-02-01 | criteria provided, single submitter | Bronchiectasis with or without elevated sweat chloride 1 |
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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
Descrption | Source | Links |
---|---|---|
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 |
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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
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