Is DSC2 p.Ser7Pro (c.19T>C) pathogenic?

DSC2 p.Ser7Pro (c.19T>C) is classified Uncertain significance in DSC2 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-05-13). AlphaMissense: likely benign (0.0636); Very rare (popmax 7.27e-05%); Associated with arrhythmogenic right ventricular dysplasia 11.

What condition is associated with DSC2 p.Ser7Pro (c.19T>C)?

DSC2 p.Ser7Pro (c.19T>C) is associated with arrhythmogenic right ventricular dysplasia 11 (ClinVar).

How common is DSC2 p.Ser7Pro (c.19T>C) in the general population?

DSC2 p.Ser7Pro (c.19T>C) is very rare (popmax 7.27e-05%) (gnomAD).

What do computational predictors say about DSC2 p.Ser7Pro (c.19T>C)?

AlphaMissense predicts likely benign (score 0.0636) — an in-silico prediction, not a clinical call.

DSC2 p.Ser7Pro

Q: How is Inherited isolated arrhythmogenic cardiomyopathy inherited?

Typically Autosomal dominant (Orphanet). A genetic counselor can assess individual risk for a family.

c.19T>C · rs774977340 · VCV1490921

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0636 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 7.27e-05%)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

arrhythmogenic right ventricular dysplasia 11

Computational evidence

Protein change
AlphaMissense	0.0636	likely benign
REVEL	0.051	moderately benign-leaning
SaProt	LLR -6.21	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP -4.3	GERP -3.2
Regional constraint	o/e 0.98	unconstrained · MANE · 34 kb · p 0.48 · regional, not allelic
Overall
CADD	0.026	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 7.27e-05%

Overall 7.27e-05% 1/1,375,098 alleles · very rare

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: DSC2
Protein: p.Ser7Pro
Coding: c.19T>C
MANE Select: NM_024422
dbSNP: rs774977340
Type: single nucleotide variant
Location: chr18:31101953 (GRCh38)
Gene constraint: LOEUF 0.743 · pLI <0.01 · ClinGen HI 1/3 (gnomAD)
Structure: AlphaFold pLDDT 77.26 · 3 PDB

Full DSC2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

arrhythmogenic right ventricular dysplasia 11 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Inherited isolated arrhythmogenic cardiomyopathy (Orphanet):

Inheritance: Autosomal dominant
Onset: No data available

Similar variants

DSC2 p.Ser7= Likely benign ★★ same residue
DSC2 p.Ser7Cys Uncertain significance ★ ⚠ same residue
DSC2 p.Ser7Phe Conflicting classifications of pathogenicity ★ ⚠ same residue
DSC3 p.Arg7Pro Uncertain significance ★ ⚠ same residue
DSC2 c.1664-1G>A Likely pathogenic ★★ same condition
DSC2 c.354+2T>A Likely pathogenic ★★ same condition
DSC2 c.355-1G>A Likely pathogenic ★★ same condition
DSC2 p.Gln554Ter Pathogenic ★★ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/dsc2-p-ser7pro (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown