Is DMD p.Pro2892= (c.8676T>C) pathogenic?

DMD p.Pro2892= (c.8676T>C) is classified Likely benign in DMD (ClinVar, Multiple submitters, 2 submitters; last evaluated 2024-11-30). Ultra-rare (popmax 0.0109%, amr); Associated with Cardiovascular phenotype.

What condition is associated with DMD p.Pro2892= (c.8676T>C)?

DMD p.Pro2892= (c.8676T>C) is associated with Cardiovascular phenotype, Duchenne muscular dystrophy (ClinVar).

How common is DMD p.Pro2892= (c.8676T>C) in the general population?

DMD p.Pro2892= (c.8676T>C) is ultra-rare (popmax 0.0109%, amr) (gnomAD).

DMD p.Pro2892=

c.8676T>C · rs757989996 · VCV1099636

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0109%, amr)

Conditions

Cardiovascular phenotype

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
REVEL	0.072	moderately benign-leaning
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP 0.15	GERP -2.4, phastCons 0.2
Overall
CADD	6.928	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0109% Admixed American · 5/45,698 alleles

Filtering AF 0.00428% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00272%

Overall 0.000579% 7/1,209,880 alleles · ultra-rare exomes 6/1,098,203 · genomes 1/111,677 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.0109%	9,140
European (non-Finnish)	0.000223%	447,654

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: DMD
Protein: p.Pro2892=
Coding: c.8676T>C
MANE Select: NM_004006
dbSNP: rs757989996
Type: single nucleotide variant
Location: chrX:31478367 (GRCh38)

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

Disease context

Cardiovascular phenotype — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Duchenne muscular dystrophy

Similar variants

DMD p.Pro2892Ser Uncertain significance ★ ⚠ same residue
DMD p.Pro2892fs Pathogenic ★ same residue
DMD c.10086+1G>A Pathogenic ★★ same condition
DMD c.10086+1G>T Pathogenic ★★ same condition
DMD c.10086+2T>C Pathogenic ★★ same condition
DMD c.10087-2A>G Pathogenic/Likely pathogenic ★★ same condition
DMD c.10223+1G>A Pathogenic ★★ same condition
DMD c.10223+1G>C 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/dmd-p-pro2892 (accessed [today's date]).

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