NM_004415.4(DSP):c.3144C>G (p.Asn1048Lys) AND Cardiovascular phenotype

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 12, 2024
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:: RCV004366662.1

Allele description [Variation Report for NM_004415.4(DSP):c.3144C>G (p.Asn1048Lys)]

NM_004415.4(DSP):c.3144C>G (p.Asn1048Lys)

Gene:

DSP:desmoplakin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p24.3

Genomic location:

Preferred name:

NM_004415.4(DSP):c.3144C>G (p.Asn1048Lys)

HGVS:

NC_000006.12:g.7579334C>G
NG_008803.1:g.42698C>G
NM_001008844.3:c.3144C>G
NM_001319034.2:c.3144C>G
NM_004415.4:c.3144C>GMANE SELECT
NP_001008844.1:p.Asn1048Lys
NP_001305963.1:p.Asn1048Lys
NP_004406.2:p.Asn1048Lys
NP_004406.2:p.Asn1048Lys
LRG_423t1:c.3144C>G
LRG_423:g.42698C>G
LRG_423p1:p.Asn1048Lys
NC_000006.11:g.7579567C>G
NM_004415.2:c.3144C>G

Protein change:

N1048K

Molecular consequence:

NM_001008844.3:c.3144C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001319034.2:c.3144C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004415.4:c.3144C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiovascular phenotype
Identifiers:: MedGen: CN230736

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005022531	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 12, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005022531

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 12, 2024)

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, SCV005022531.1

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

Description

The p.N1048K variant (also known as c.3144C>G), located in coding exon 23 of the DSP gene, results from a C to G substitution at nucleotide position 3144. The asparagine at codon 1048 is replaced by lysine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Based on the available evidence, 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

ClinVar

Relating variation to medicine