NM_004415.4(DSP):c.7876G>C (p.Glu2626Gln) AND Cardiovascular phenotype

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 14, 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:: RCV003166041.2

Allele description [Variation Report for NM_004415.4(DSP):c.7876G>C (p.Glu2626Gln)]

NM_004415.4(DSP):c.7876G>C (p.Glu2626Gln)

Gene:

DSP:desmoplakin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p24.3

Genomic location:

Preferred name:

NM_004415.4(DSP):c.7876G>C (p.Glu2626Gln)

HGVS:

NC_000006.12:g.7585138G>C
NG_008803.1:g.48502G>C
NM_001008844.3:c.6079G>C
NM_001319034.2:c.6547G>C
NM_004415.4:c.7876G>CMANE SELECT
NP_001008844.1:p.Glu2027Gln
NP_001305963.1:p.Glu2183Gln
NP_004406.2:p.Glu2626Gln
LRG_423t1:c.7876G>C
LRG_423:g.48502G>C
NC_000006.11:g.7585371G>C
NM_004415.2:c.7876G>C

Protein change:

E2027Q

Links:

dbSNP: rs144821643

NCBI 1000 Genomes Browser:

rs144821643

Molecular consequence:

NM_001008844.3:c.6079G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001319034.2:c.6547G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_004415.4:c.7876G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiovascular phenotype
Identifiers:: MedGen: CN230736

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003867551	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Nov 14, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003867551

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Nov 14, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003867551.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The p.E2626Q variant (also known as c.7876G>C), located in coding exon 24 of the DSP gene, results from a G to C substitution at nucleotide position 7876. The glutamic acid at codon 2626 is replaced by glutamine, an amino acid with highly similar properties. This amino acid position is conserved. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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