Is ACTL7B p.Ser210Phe (c.629C>T) pathogenic?

ACTL7B p.Ser210Phe (c.629C>T) is classified Uncertain significance in ACTL7B (ClinVar, Single submitter, 1 submitter; last evaluated 2022-07-06). AlphaMissense: likely benign (0.1314); Absent from gnomAD v4.1.

How common is ACTL7B p.Ser210Phe (c.629C>T) in the general population?

ACTL7B p.Ser210Phe (c.629C>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about ACTL7B p.Ser210Phe (c.629C>T)?

AlphaMissense predicts likely benign (score 0.1314) — an in-silico prediction, not a clinical call.

ACTL7B p.Ser210Phe

c.629C>T · rs758565813 · VCV2299837

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1314 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/2 damaging

AlphaMissense, SaProt · REVEL no call

Computational evidence

Protein change
AlphaMissense	0.1314	likely benign
REVEL	0.567	indeterminate
SaProt	LLR -2.98	tolerated
⇒ AlphaMissense and SaProt both call this tolerated; REVEL makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 3.3	GERP -0.24, phastCons 1
Regional constraint	o/e 1.04	unconstrained · MANE · 1,244 bp · p 0.29 · regional, not allelic
Overall
CADD	23.2	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

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: ACTL7B
Protein: p.Ser210Phe
Coding: c.629C>T
MANE Select: NM_006686
dbSNP: rs758565813
Type: single nucleotide variant
Location: chr9:108855302 (GRCh38)
Gene constraint: LOEUF 1.414 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 88.35

Full ACTL7B gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

ACTL7B p.Ala263= Benign ★★ same type
ACTL7B p.Ala164Thr Uncertain significance ★ ⚠ same type
ACTL7B p.Ala240Val Uncertain significance ★ ⚠ same type
ACTL7B p.Ala243Thr Uncertain significance ★ ⚠ same type
ACTL7B p.Ala28Val Uncertain significance ★ ⚠ same type
ACTL7B p.Ala2Val Uncertain significance ★ ⚠ same type
ACTL7B p.Ala36Gly Uncertain significance ★ ⚠ same type
ACTL7B p.Ala388Ser Uncertain significance ★ ⚠ same type

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/actl7b-p-ser210phe (accessed [today's date]).

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