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NM_001943.5(DSG2):c.2510C>A (p.Ala837Asp) AND Cardiovascular phenotype

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 4, 2022
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:
RCV003159997.2

Allele description [Variation Report for NM_001943.5(DSG2):c.2510C>A (p.Ala837Asp)]

NM_001943.5(DSG2):c.2510C>A (p.Ala837Asp)

Genes:
DSG2-AS1:DSG2 antisense RNA 1 [Gene - HGNC]
DSG2:desmoglein 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
18q12.1
Genomic location:
Preferred name:
NM_001943.5(DSG2):c.2510C>A (p.Ala837Asp)
HGVS:
  • NC_000018.10:g.31545896C>A
  • NG_007072.3:g.52655C>A
  • NM_001943.5:c.2510C>AMANE SELECT
  • NP_001934.2:p.Ala837Asp
  • LRG_397t1:c.2510C>A
  • LRG_397:g.52655C>A
  • NC_000018.9:g.29125859C>A
  • NM_001943.3:c.2510C>A
  • NM_001943.4:c.2510C>A
  • NR_045216.1:n.1356G>T
Protein change:
A837D
Links:
dbSNP: rs756338201
NCBI 1000 Genomes Browser:
rs756338201
Molecular consequence:
  • NM_001943.5:c.2510C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_045216.1:n.1356G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

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
SCV003859081Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Dec 4, 2022) 		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, SCV003859081.2

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

Description

The p.A837D variant (also known as c.2510C>A), located in coding exon 15 of the DSG2 gene, results from a C to A substitution at nucleotide position 2510. The alanine at codon 837 is replaced by aspartic acid, an amino acid with dissimilar 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