Is PMS2 p.Ala765Ser (c.2293G>T) pathogenic?

PMS2 p.Ala765Ser (c.2293G>T) is classified Uncertain significance in PMS2 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-02-27). AlphaMissense: likely benign (0.3335); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with PMS2 p.Ala765Ser (c.2293G>T)?

PMS2 p.Ala765Ser (c.2293G>T) is associated with hereditary neoplastic syndrome (ClinVar).

How common is PMS2 p.Ala765Ser (c.2293G>T) in the general population?

PMS2 p.Ala765Ser (c.2293G>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about PMS2 p.Ala765Ser (c.2293G>T)?

AlphaMissense predicts likely benign (score 0.3335) — an in-silico prediction, not a clinical call.

PMS2 p.Ala765Ser

c.2293G>T · VCV3891010

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.3335 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/2 damaging

AlphaMissense, SaProt · REVEL no call

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.3335	likely benign
REVEL	0.311	indeterminate
SaProt	LLR -8.17	tolerated
⇒ AlphaMissense and SaProt both call this tolerated; REVEL makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Pangolin	Δ0.22	gain · loss 0.09 · not in the SpliceAI release · independent
Constraint at this position
Conservation	phyloP 5.9	phastCons 1
Regional constraint	o/e 0.40	unconstrained · MANE · 13 kb · p 2e-20 · regional, not allelic
Overall
CADD	24.7	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: PMS2
Protein: p.Ala765Ser
Coding: c.2293G>T
MANE Select: NM_000535
Type: single nucleotide variant
Location: chr7:5977740 (GRCh38)
Gene constraint: LOEUF 0.898 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 71.37 · 9 PDB

Full PMS2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

hereditary neoplastic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

PMS2 p.Ala765Asp Uncertain significance ★★ ⚠ same residue
PMS2 p.Ala765= Benign/Likely benign ★★ same residue
PMS2 p.Ala765Val Uncertain significance ★ ⚠ same residue
PMS2 p.Ala765Gly Uncertain significance ★ same residue
PMS2 p.Ala765Pro Uncertain significance ★ ⚠ same residue
PMS2 p.Ala765Thr Uncertain significance ★ ⚠ same residue
PMS2 c.163+2T>C Likely pathogenic ★★★ same condition
PMS2 c.164-2A>G Likely 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/pms2-p-ala765ser (accessed [today's date]).

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