Is ATAD3A p.Arg273Pro (c.818G>C) pathogenic?

ATAD3A p.Arg273Pro (c.818G>C) is classified Uncertain significance in ATAD3A (ClinVar, Single submitter, 1 submitter; last evaluated 2022-05-04). AlphaMissense: likely pathogenic (0.8266); Absent from gnomAD v4.1; Associated with Inborn genetic diseases.

What condition is associated with ATAD3A p.Arg273Pro (c.818G>C)?

ATAD3A p.Arg273Pro (c.818G>C) is associated with Inborn genetic diseases (ClinVar).

How common is ATAD3A p.Arg273Pro (c.818G>C) in the general population?

ATAD3A p.Arg273Pro (c.818G>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about ATAD3A p.Arg273Pro (c.818G>C)?

AlphaMissense predicts likely pathogenic (score 0.8266) — an in-silico prediction, not a clinical call.

ATAD3A p.Arg273Pro

c.818G>C · rs779686128 · VCV2287425

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.8266 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

2/2 damaging

AlphaMissense, REVEL

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.8266	likely pathogenic
REVEL	0.771	pathogenic-leaning
⇒ AlphaMissense and REVEL both call this damaging.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 9.6	GERP 1.5, phastCons 1
Regional constraint	o/e 0.94	unconstrained · MANE · 6,537 bp · p 0.3 · regional, not allelic
Overall
CADD	25.9	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean damaging — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

⚠ Isoform check: AlphaMissense numbered on a different transcript (AM R321P vs ClinVar R273P) — verify the residue.

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: ATAD3A
Protein: p.Arg273Pro
Coding: c.818G>C
MANE Select: NM_001170535
dbSNP: rs779686128
Type: single nucleotide variant
Location: chr1:1522811 (GRCh38)
Gene constraint: LOEUF 0.861 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 82.35
Residue 273: a UniProt-annotated variant site (in phrinl)

Full ATAD3A 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

ATAD3A p.Arg273Cys Uncertain significance ★★ ⚠ same residue
ATAD3A p.Arg273His Uncertain significance ★ ⚠ same residue
ATAD3A p.Arg273Ser Uncertain significance ★★ ⚠ same residue
ATAD3A p.Arg273Leu Uncertain significance ★ ⚠ same residue
ATAD3A p.Ala62Val Uncertain significance ★★ ⚠ same condition
ATAD3A p.Arg138Trp Uncertain significance ★★ same condition
ATAD3A p.Arg188Gln Uncertain significance ★★ ⚠ same condition
ATAD3A p.Arg208Cys 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/atad3a-p-arg273pro (accessed [today's date]).

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