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NM_001009944.3(PKD1):c.2289_2299del (p.Cys767fs)

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Interpretation:
Likely pathogenic​

Review status:
criteria provided, single submitter
Submissions:
1 (Most recent: Jun 21, 2020)
Last evaluated:
Jan 1, 2019
Accession:
VCV000972848.1
Variation ID:
972848
Description:
11bp deletion
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NM_001009944.3(PKD1):c.2289_2299del (p.Cys767fs)

Allele ID
961191
Variant type
Deletion
Variant length
11 bp
Cytogenetic location
16p13.3
Genomic location
16: 2114724-2114734 (GRCh38) GRCh38 UCSC
16: 2164725-2164735 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000016.10:g.2114724_2114734del
NC_000016.9:g.2164725_2164735del
NM_001009944.3:c.2289_2299del MANE Select NP_001009944.3:p.Cys767fs frameshift
... more HGVS
Protein change
C767fs
Other names
-
Canonical SPDI
NC_000016.10:2114723:AGGCAGGGCAG:
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 RCV001249128.1
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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: clinical testing
not provided
Allele origin: germline
Molecular Genetics of Inherited Kidney Disorders Laboratory,Garvan Institute of Medical Research
Accession: SCV001422401.1
Submitted: (Jun 21, 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 Aug 01, 2020