18-31074729-AC-A

Variant names:

• chr18-31074729-AC-A
• rs397514043
• NM_024422.6:c.1841delG

Variant summary

Our verdict is Pathogenic. The variant received 11 ACMG points: 11P and 0B. PVS1 PM2 PP5

The NM_024422.6(DSC2):​c.1841delG​(p.Ser614IlefsTer12) variant causes a frameshift change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (no stars). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 32)
• Consequence: DSC2 NM_024422.6 frameshift
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 0.0120
• Publications: 4 publications found

Genes affected

DSC2 (HGNC:3036): (desmocollin 2) This gene encodes a member of the desmocollin protein subfamily. Desmocollins, along with desmogleins, are cadherin-like transmembrane glycoproteins that are major components of the desmosome. Desmosomes are cell-cell junctions that help resist shearing forces and are found in high concentrations in cells subject to mechanical stress. This gene is found in a cluster with other desmocollin family members on chromosome 18. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia-11, and reduced protein expression has been described in several types of cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]

DSC2 Gene-Disease associations (from GenCC):

• familial isolated arrhythmogenic right ventricular dysplasia

  Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen
• arrhythmogenic right ventricular dysplasia 11

  Inheritance: AR, AD, SD Classification: DEFINITIVE, STRONG, LIMITED Submitted by: Genomics England PanelApp, Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics
• colorectal adenoma

  Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics

ACMG classification

Our verdict: Pathogenic. The variant received 11 ACMG points.

• PVS1: Loss of function variant, product undergoes nonsense mediated mRNA decay. LoF is a known mechanism of disease.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 18-31074729-AC-A is Pathogenic according to our data. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31074729-AC-A is described in CliVar as Pathogenic. Clinvar id is 31635.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DSC2	NM_024422.6	c.1841delG	p.Ser614IlefsTer12	frameshift_variant	Exon 12 of 16	ENST00000280904.11	NP_077740.1
DSC2	NM_004949.5	c.1841delG	p.Ser614IlefsTer12	frameshift_variant	Exon 12 of 17		NP_004940.1
DSC2	NM_001406506.1	c.1412delG	p.Ser471IlefsTer12	frameshift_variant	Exon 12 of 16		NP_001393435.1
DSC2	NM_001406507.1	c.1412delG	p.Ser471IlefsTer12	frameshift_variant	Exon 12 of 17		NP_001393436.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DSC2	ENST00000280904.11	c.1841delG	p.Ser614IlefsTer12	frameshift_variant	Exon 12 of 16	1	NM_024422.6	ENSP00000280904.6

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Pathogenic:1

Jan 01, 2009

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.012
Mutation Taster		=1/199	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.020		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs397514043; hg19: chr18-28654695;