Is PGAM2 p.Asp202Glu (c.606C>G) pathogenic?

PGAM2 p.Asp202Glu (c.606C>G) is classified Uncertain significance in PGAM2 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-10-22). AlphaMissense: likely benign (0.1958); Absent from gnomAD v4.1; Associated with Inborn genetic diseases.

What condition is associated with PGAM2 p.Asp202Glu (c.606C>G)?

PGAM2 p.Asp202Glu (c.606C>G) is associated with Inborn genetic diseases (ClinVar).

How common is PGAM2 p.Asp202Glu (c.606C>G) in the general population?

PGAM2 p.Asp202Glu (c.606C>G) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about PGAM2 p.Asp202Glu (c.606C>G)?

AlphaMissense predicts likely benign (score 0.1958) — an in-silico prediction, not a clinical call.

PGAM2 p.Asp202Glu

c.606C>G · VCV4627330

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1958 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.1958	likely benign
REVEL	0.258	benign-leaning
SaProt	LLR -6.69	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not looked up on this page · why
Constraint at this position
Conservation	phyloP 0.77	GERP -2.1, phastCons 1
Regional constraint	o/e 0.98	unconstrained · MANE · 2,762 bp · p 0.7 · regional, not allelic
Overall
CADD	12.65	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: PGAM2
Protein: p.Asp202Glu
Coding: c.606C>G
MANE Select: NM_001014436 · reported on NM_000290
Type: single nucleotide variant
Location: chr7:44062920 (GRCh38)

Full PGAM2 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

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/pgam2-p-asp202glu (accessed [today's date]).

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