NM_024422.6:c.1430delC

Variant names:

Variant summary

Our verdict is Pathogenic. The variant received 11 ACMG points: 11P and 0B. PVS1PM2PP5

The NM_024422.6(DSC2):c.1430delC(p.Thr477MetfsTer4) variant causes a frameshift change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000137 in 1,461,836 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Pathogenic (no stars). Synonymous variant affecting the same amino acid position (i.e. T477T) has been classified as Likely benign. Variant results in nonsense mediated mRNA decay.

Frequency

Genomes: not found (cov: 33)

Exomes 𝑓: 0.0000014 ( 0 hom. )

Consequence

DSC2
NM_024422.6 frameshift

Scores

Not classified

Clinical Significance

Pathogenic no assertion criteria provided P:1

Conservation

PhyloP100: -0.472

Publications

3 publications found

Variant links:

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

DSC2 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

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 18-31080185-AG-A is Pathogenic according to our data. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr18-31080185-AG-A is described in CliVar as Pathogenic. Clinvar id is 16848.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 link	c.1430delC	p.Thr477MetfsTer4	frameshift_variant	Exon 10 of 16	ENST00000280904.11	NP_077740.1	Q02487-1
DSC2	NM_004949.5 link	c.1430delC	p.Thr477MetfsTer4	frameshift_variant	Exon 10 of 17		NP_004940.1	Q02487-2
DSC2	NM_001406506.1 link	c.1001delC	p.Thr334MetfsTer4	frameshift_variant	Exon 10 of 16		NP_001393435.1
DSC2	NM_001406507.1 link	c.1001delC	p.Thr334MetfsTer4	frameshift_variant	Exon 10 of 17		NP_001393436.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DSC2	ENST00000280904.11 link	c.1430delC	p.Thr477MetfsTer4	frameshift_variant	Exon 10 of 16	1	NM_024422.6	ENSP00000280904.6		Q02487-1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

0.00000137

AC:

AN:

1461836

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

727220

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

33480

American (AMR)

AF:

0.00

AC:

AN:

44718

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26132

East Asian (EAS)

AF:

0.00

AC:

AN:

39690

South Asian (SAS)

AF:

0.00

AC:

AN:

86258

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53406

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.00000180

AC:

AN:

1111994

Other (OTH)

AF:

0.00

AC:

AN:

60390

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.425

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

Cov.:

Alfa

AF:

0.00

Hom.:

Bravo

AF:

0.00000378

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

Arrhythmogenic right ventricular dysplasia 11

Pathogenic:1

Nov 01, 2006

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

-0.47

Mutation Taster

=0/200

disease causing (ClinVar)

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.14

Details are displayed if max score is > 0.2

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

Publications

You must be logged in to view publications. This limit was set because tens of millions (!) of queries from AI bots are generated daily.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over