Is CSRP3 p.Ser95Phe (c.284C>T) pathogenic?

CSRP3 p.Ser95Phe (c.284C>T) is classified Uncertain significance in CSRP3 (ClinVar, Multiple submitters, 3 submitters; last evaluated 2025-10-27). AlphaMissense: likely benign (0.1392); Ultra-rare (popmax 0.0535%, eas); Associated with Cardiovascular phenotype.

What condition is associated with CSRP3 p.Ser95Phe (c.284C>T)?

CSRP3 p.Ser95Phe (c.284C>T) is associated with Cardiovascular phenotype, dilated cardiomyopathy 1M, hypertrophic cardiomyopathy 12 (ClinVar).

How common is CSRP3 p.Ser95Phe (c.284C>T) in the general population?

CSRP3 p.Ser95Phe (c.284C>T) is ultra-rare (popmax 0.0535%, eas) (gnomAD).

What do computational predictors say about CSRP3 p.Ser95Phe (c.284C>T)?

AlphaMissense predicts likely benign (score 0.1392) — an in-silico prediction, not a clinical call.

CSRP3 p.Ser95Phe

c.284C>T · rs767477787 · VCV863545

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

AlphaMissense

likely benign

0.1392 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0535%, eas)

Missense predictors

1/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Cardiovascular phenotype

Computational evidence

Protein change
AlphaMissense	0.1392	likely benign
REVEL	0.215	benign-leaning
SaProt	LLR -10.24	damaging
⇒ SaProt calls this damaging; AlphaMissense and REVEL do not.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 12	phastCons 1
Regional constraint	o/e 0.96	unconstrained · MANE · 9,775 bp · p 0.57 · regional, not allelic
Overall
CADD	25.7	PHRED · no single calibrated threshold — expert panels disagree

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0535% East Asian · 24/44,878 alleles

Filtering AF 0.0368% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0313%

Overall 0.00171% 25/1,461,886 alleles · ultra-rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.0535%	1,870
Ashkenazi Jewishnot grpmax-eligible	0.00338%	29,608

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: CSRP3
Protein: p.Ser95Phe
Coding: c.284C>T
MANE Select: NM_003476
dbSNP: rs767477787
Type: single nucleotide variant
Location: chr11:19186346 (GRCh38)
Gene constraint: LOEUF 1.307 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 73.91 · 2 PDB
Residue 95: the 'interaction with clf2 and isoform 2' region; a modified residue (phosphoserine)

Full CSRP3 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 1M hypertrophic cardiomyopathy 12

Similar variants

CSRP3 p.Ser95Ala Uncertain significance ★★ ⚠ same residue
CSRP3 p.Ser95Cys Uncertain significance ★ ⚠ same residue
CSRP3 p.Ser95= Likely benign ★ same residue
CSRP3 c.414+1G>T Likely pathogenic ★★ same condition
CSRP3 p.Cys37Ter Pathogenic/Likely pathogenic ★★ same condition
CSRP3 p.Cys58Gly Pathogenic ★★ same condition
CSRP3 p.Lys113Ter Pathogenic ★★ same condition
CSRP3 c.113-3C>T 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/csrp3-p-ser95phe (accessed [today's date]).

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