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NM_001009944.3(PKD1):c.9502_9504del (p.Phe3168del)

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Interpretation:
Likely pathogenic​

Review status:
criteria provided, single submitter
Submissions:
1 (Most recent: Aug 18, 2020)
Last evaluated:
Jan 1, 2019
Accession:
VCV000976803.1
Variation ID:
976803
Description:
3bp deletion
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NM_001009944.3(PKD1):c.9502_9504del (p.Phe3168del)

Allele ID
964945
Variant type
Deletion
Variant length
3 bp
Cytogenetic location
16p13.3
Genomic location
16: 2100460-2100462 (GRCh38) GRCh38 UCSC
16: 2150461-2150463 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000016.10:g.2100462_2100464del
NC_000016.9:g.2150463_2150465del
NG_008617.1:g.42759_42761del
... more HGVS
Protein change
F3168del
Other names
-
Canonical SPDI
NC_000016.10:2100459:GAAGA:GA
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
-
Links
VarSome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Likely pathogenic 1 criteria provided, single submitter Jan 1, 2019 RCV001254211.1

Clinical features observed in individuals with this variant

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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
PKD1 Sufficient evidence for dosage pathogenicity No evidence available GRCh38
GRCh38
GRCh37
1761 2100

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Likely pathogenic
(Jan 01, 2019)
criteria provided, single submitter
Method: research
Autosomal dominant polycystic kidney disease
Allele origin: germline
Molecular Genetics of Inherited Kidney Disorders Laboratory,Garvan Institute of Medical Research
Accession: SCV001430280.1
Submitted: (Aug 18, 2020)
Evidence details

Functional evidence

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There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for this variant

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There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar.

Record last updated Oct 08, 2021