Is MSH3 p.Phe27Val (c.79T>G) pathogenic?

MSH3 p.Phe27Val (c.79T>G) is classified Uncertain significance in MSH3 (ClinVar, Multiple submitters, 3 submitters; last evaluated 2025-07-02). AlphaMissense: ambiguous (0.4295); Very rare (popmax 0.00136%, afr); Associated with hereditary neoplastic syndrome.

What condition is associated with MSH3 p.Phe27Val (c.79T>G)?

MSH3 p.Phe27Val (c.79T>G) is associated with hereditary neoplastic syndrome (ClinVar).

How common is MSH3 p.Phe27Val (c.79T>G) in the general population?

MSH3 p.Phe27Val (c.79T>G) is very rare (popmax 0.00136%, afr) (gnomAD).

What do computational predictors say about MSH3 p.Phe27Val (c.79T>G)?

AlphaMissense predicts ambiguous (score 0.4295) — an in-silico prediction, not a clinical call.

MSH3 p.Phe27Val

c.79T>G · rs1465875645 · VCV1060565

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

AlphaMissense

ambiguous

0.4295 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00136%, afr)

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.4295	ambiguous
REVEL	0.624	indeterminate
SaProt	LLR -12.85	damaging
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.5	GERP 1.9, phastCons 1
Regional constraint	o/e 1.08	unconstrained · MANE · 221 kb · p 0.0024 · regional, not allelic
Overall
CADD	28.1	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 0.00136% African / African-American · 1/73,594 alleles

Overall 6.22e-05% 1/1,606,886 alleles · very rare exomes 0/1,455,118 · genomes 1/151,768 · joint denominator

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: MSH3
Protein: p.Phe27Val
Coding: c.79T>G
MANE Select: NM_002439
dbSNP: rs1465875645
Type: single nucleotide variant
Location: chr5:80654806 (GRCh38)
Gene constraint: LOEUF 1.027 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 79.48 · 25 PDB

Full MSH3 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

MSH3 p.Phe27Leu Uncertain significance ★ ⚠ same residue
MSH3 c.1341-2A>C Likely pathogenic ★★ same condition
MSH3 c.1341-2A>G Likely pathogenic ★★ same condition
MSH3 c.1568+1G>C Likely pathogenic ★★ same condition
MSH3 c.1653+1G>A Likely pathogenic ★★ same condition
MSH3 c.1764-1G>A Pathogenic/Likely pathogenic ★★ same condition
MSH3 c.1764-2A>C Pathogenic/Likely pathogenic ★★ same condition
MSH3 c.1764-2A>G Pathogenic/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/msh3-p-phe27val (accessed [today's date]).

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