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NM_015404.4(WHRN):c.1992G>A (p.Pro664=)

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Interpretation:
Conflicting interpretations of pathogenicity​

Benign(1);Likely benign(1);Uncertain significance(2)

Review status:
criteria provided, conflicting interpretations
Submissions:
5 (Most recent: Aug 20, 2021)
Last evaluated:
Nov 17, 2020
Accession:
VCV000178336.7
Variation ID:
178336
Description:
single nucleotide variant
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NM_015404.4(WHRN):c.1992G>A (p.Pro664=)

Allele ID
174545
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
9q32
Genomic location
9: 114406599 (GRCh38) GRCh38 UCSC
9: 117168879 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000009.11:g.117168879C>T
NC_000009.12:g.114406599C>T
NM_015404.4:c.1992G>A MANE Select NP_056219.3:p.Pro664= synonymous
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000009.12:114406598:C:T
Functional consequence
-
Global minor allele frequency (GMAF)
0.00200 (T)

Allele frequency
The Genome Aggregation Database (gnomAD), exomes 0.00024
Trans-Omics for Precision Medicine (TOPMed) 0.00088
The Genome Aggregation Database (gnomAD) 0.00070
1000 Genomes Project 0.00200
NHLBI Exome Sequencing Project (ESP) Exome Variant Server 0.00046
Exome Aggregation Consortium (ExAC) 0.00028
Links
ClinGen: CA182132
dbSNP: rs142568702
Varsome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Likely benign 1 criteria provided, single submitter Nov 24, 2015 RCV000155080.2
Uncertain significance 1 criteria provided, single submitter Jan 13, 2018 RCV000308124.2
Uncertain significance 1 criteria provided, single submitter Jan 13, 2018 RCV000393724.2
Benign 2 criteria provided, single submitter Nov 17, 2020 RCV000907763.4
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
WHRN - - GRCh38
GRCh37
437 477

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Likely benign
(Nov 24, 2015)
criteria provided, single submitter
Method: clinical testing
not specified
Allele origin: germline
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine
Accession: SCV000204764.5
Submitted: (Mar 21, 2019)
Evidence details
Comment:
p.Pro664Pro in Exon 9 of DFNB31: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue, … (more)
Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
Method: clinical testing
Deafness, autosomal recessive 31
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000476749.3
Submitted: (Feb 20, 2020)
Evidence details
Comment:
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated … (more)
Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
Method: clinical testing
Usher syndrome, type 2D
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000476748.3
Submitted: (Feb 20, 2020)
Evidence details
Comment:
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated … (more)
Benign
(Nov 17, 2020)
criteria provided, single submitter
Method: clinical testing
not provided
Allele origin: germline
Invitae
Accession: SCV001052488.3
Submitted: (Jan 07, 2021)
Evidence details
Likely benign
(Apr 14, 2020)
no assertion criteria provided
Method: clinical testing
Not Provided
Allele origin: germline
GeneDx
Accession: SCV001803942.1
Submitted: (Aug 20, 2021)
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.

Text-mined citations for rs142568702...

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These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Aug 24, 2021