Is ACTN2 p.Ser886= (c.2658C>T) pathogenic?

ACTN2 p.Ser886= (c.2658C>T) is classified Likely benign in ACTN2 (ClinVar, Multiple submitters, 3 submitters; last evaluated 2026-01-18). Ultra-rare (popmax 0.0154%, sas); Associated with Cardiovascular phenotype.

What condition is associated with ACTN2 p.Ser886= (c.2658C>T)?

ACTN2 p.Ser886= (c.2658C>T) is associated with Cardiovascular phenotype, dilated cardiomyopathy 1AA, familial hypertrophic cardiomyopathy (ClinVar).

How common is ACTN2 p.Ser886= (c.2658C>T) in the general population?

ACTN2 p.Ser886= (c.2658C>T) is ultra-rare (popmax 0.0154%, sas) (gnomAD).

ACTN2 p.Ser886=

c.2658C>T · rs143297401 · VCV263591

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0154%, sas)

Conditions

Cardiovascular phenotype

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP -11	GERP -5.7
Overall
CADD	0.551	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0154% South Asian · 14/91,070 alleles

Filtering AF 0.0092% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00735%

Overall 0.0039% 63/1,614,080 alleles · ultra-rare exomes 55/1,461,840 · genomes 8/152,240 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.0154%	6,505
African / African-American	0.008%	12,504
European (non-Finnish)	0.00347%	28,780
Admixed American	0.00167%	60,018
Remaining individualsnot grpmax-eligible	0.0016%	62,506

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: ACTN2
Protein: p.Ser886=
Coding: c.2658C>T
MANE Select: NM_001103
dbSNP: rs143297401
Type: single nucleotide variant
Location: chr1:236762592 (GRCh38)
Gene constraint: LOEUF 0.432 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 84.88 · 18 PDB
Residue 886: an α-helix

Full ACTN2 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: dilated cardiomyopathy 1AA familial hypertrophic cardiomyopathy

Similar variants

ACTN2 p.Ser886Pro Uncertain significance ★★ ⚠ same residue
ACTN2 p.Ser886Phe Uncertain significance ★ ⚠ same residue
ACTN2 p.Ala119Thr Pathogenic/Likely pathogenic ★★ ⚠ same condition
ACTN2 p.Thr247Met Likely pathogenic ★★ same condition
ACTN2 c.1107+3G>A Uncertain significance ★★ same condition
ACTN2 c.1108-10A>G Uncertain significance ★★ same condition
ACTN2 c.1255+1G>C Uncertain significance ★★ same condition
ACTN2 c.126+2T>G Uncertain significance ★★ 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/actn2-p-ser886 (accessed [today's date]).

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