NM_004415.4(DSP):c.105G>A (p.Gly35=) AND Cardiomyopathy

Germline classification:: Benign (2 submissions)
Last evaluated:: Mar 14, 2018
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:: RCV000029675.11

Allele description [Variation Report for NM_004415.4(DSP):c.105G>A (p.Gly35=)]

NM_004415.4(DSP):c.105G>A (p.Gly35=)

Genes:

DSP-AS1:DSP antisense RNA 1 [Gene - HGNC]
DSP:desmoplakin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p24.3

Genomic location:

Preferred name:

NM_004415.4(DSP):c.105G>A (p.Gly35=)

HGVS:

NC_000006.12:g.7542020G>A
NG_008803.1:g.5384G>A
NM_001008844.3:c.105G>A
NM_001319034.2:c.105G>A
NM_004415.4:c.105G>AMANE SELECT
NP_001008844.1:p.Gly35=
NP_001305963.1:p.Gly35=
NP_004406.2:p.Gly35=
LRG_423t1:c.105G>A
LRG_423:g.5384G>A
NC_000006.11:g.7542253G>A
NM_004415.2:c.105G>A
NP_004406.2:p.(=)
c.105G>A

Links:

dbSNP: rs77445784

NCBI 1000 Genomes Browser:

rs77445784

Molecular consequence:

NM_001008844.3:c.105G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001319034.2:c.105G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_004415.4:c.105G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Cardiomyopathy (CMYO)
Synonyms:: Cardiomyopathies
Identifiers:: MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000052327	Women's Health and Genetics/Laboratory Corporation of America, LabCorp	no assertion criteria provided	Benign (May 13, 2015)	germline	clinical testing
SCV000902763	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Mar 14, 2018)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000052327

Women's Health and Genetics/Laboratory Corporation of America, LabCorp

no assertion criteria provided

Benign
(May 13, 2015)

germline

clinical testing

SCV000902763

Color Diagnostics, LLC DBA Color Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Mar 14, 2018)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Women's Health and Genetics/Laboratory Corporation of America, LabCorp, SCV000052327.2

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

#	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

From Color Diagnostics, LLC DBA Color Health, SCV000902763.1

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

#	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: Nov 24, 2024

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