Is MDH2 p.Arg14Pro (c.41G>C) pathogenic?

MDH2 p.Arg14Pro (c.41G>C) is classified Uncertain significance in MDH2 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-10-31). AlphaMissense: likely benign (0.2276); Absent from gnomAD v4.1; Associated with Inborn genetic diseases.

What condition is associated with MDH2 p.Arg14Pro (c.41G>C)?

MDH2 p.Arg14Pro (c.41G>C) is associated with Inborn genetic diseases (ClinVar).

How common is MDH2 p.Arg14Pro (c.41G>C) in the general population?

MDH2 p.Arg14Pro (c.41G>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about MDH2 p.Arg14Pro (c.41G>C)?

AlphaMissense predicts likely benign (score 0.2276) — an in-silico prediction, not a clinical call.

MDH2 p.Arg14Pro

c.41G>C · VCV3394055

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.2276 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

1/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.2276	likely benign
REVEL	0.118	moderately benign-leaning
SaProt	LLR -11.07	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 9.3	phastCons 1
Regional constraint	o/e 0.97	unconstrained · MANE · 18 kb · p 0.54 · regional, not allelic
Overall
CADD	25.6	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

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: MDH2
Protein: p.Arg14Pro
Coding: c.41G>C
MANE Select: NM_005918
Type: single nucleotide variant
Location: chr7:76048201 (GRCh38)
Gene constraint: LOEUF 0.984 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 93.49 · 7 PDB

Full MDH2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

MDH2 p.Arg14= Likely benign ★★ same residue
MDH2 p.Arg14Cys Uncertain significance ★ ⚠ same residue
MDH2 p.Arg14Gly Uncertain significance ★ ⚠ same residue
MDH2 p.Arg14His Uncertain significance ★ ⚠ same residue
MDH2 p.Ala135Gly Uncertain significance ★★ ⚠ same condition
MDH2 p.Ala141Thr Uncertain significance ★★ same condition
MDH2 p.Ala177Thr Uncertain significance ★★ ⚠ same condition
MDH2 p.Ala21Val 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/mdh2-p-arg14pro (accessed [today's date]).

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