Is EMID1 p.Pro183Arg (c.548C>G) pathogenic?

EMID1 p.Pro183Arg (c.548C>G) is classified Uncertain significance in EMID1 (ClinVar, Single submitter, 1 submitter; last evaluated 2023-10-10). Very rare (popmax 0.00446%, eas).

How common is EMID1 p.Pro183Arg (c.548C>G) in the general population?

EMID1 p.Pro183Arg (c.548C>G) is very rare (popmax 0.00446%, eas) (gnomAD).

EMID1 p.Pro183Arg

c.548C>G · rs767206038 · VCV3088583

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00446%, eas)

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
REVEL	0.309	indeterminate
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 3.2	GERP -0.63, phastCons 0.99
Regional constraint	o/e 0.98	unconstrained · MANE · 53 kb · p 0.62 · regional, not allelic
Overall
CADD	22.1	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00446% East Asian · 2/44,886 alleles

Filtering AF 0.000739% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000276%

Overall 0.000124% 2/1,613,152 alleles · very rare

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: EMID1
Protein: p.Pro183Arg
Coding: c.548C>G
MANE Select: NM_133455
dbSNP: rs767206038
Type: single nucleotide variant
Location: chr22:29231102 (GRCh38)
Gene constraint: LOEUF 0.994 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 51.77
Residue 183: the collagen-like domain; the 'disordered' region

Full EMID1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

EMID1 c.587-5C>G Benign ★★ same type
EMID1 p.Ala108Thr Uncertain significance ★ same type
EMID1 p.Ala112Thr Uncertain significance ★ same type
EMID1 p.Ala127Ser Uncertain significance ★ same type
EMID1 p.Ala28Thr Uncertain significance ★ same type
EMID1 p.Ala409Val Uncertain significance ★ same type
EMID1 p.Ala435Asp Uncertain significance ★ same type
EMID1 p.Ala6Ser Uncertain significance ★ same type

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/emid1-p-pro183arg (accessed [today's date]).

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