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NM_001943.5(DSG2):c.1489C>A (p.Pro497Thr) AND Cardiovascular phenotype

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 10, 2021
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV002388308.2

Allele description [Variation Report for NM_001943.5(DSG2):c.1489C>A (p.Pro497Thr)]

NM_001943.5(DSG2):c.1489C>A (p.Pro497Thr)

Gene:
DSG2:desmoglein 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
18q12.1
Genomic location:
Preferred name:
NM_001943.5(DSG2):c.1489C>A (p.Pro497Thr)
HGVS:
  • NC_000018.10:g.31536267C>A
  • NG_007072.3:g.43026C>A
  • NM_001943.5:c.1489C>AMANE SELECT
  • NP_001934.2:p.Pro497Thr
  • LRG_397t1:c.1489C>A
  • LRG_397:g.43026C>A
  • NC_000018.9:g.29116230C>A
  • NM_001943.3:c.1489C>A
Protein change:
P497T
Links:
dbSNP: rs1293179210
NCBI 1000 Genomes Browser:
rs1293179210
Molecular consequence:
  • NM_001943.5:c.1489C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002702675Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Aug 10, 2021) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV002702675.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The p.P497T variant (also known as c.1489C>A), located in coding exon 11 of the DSG2 gene, results from a C to A substitution at nucleotide position 1489. The proline at codon 497 is replaced by threonine, an amino acid with highly similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024