Is ERCC4 p.Ile73Val (c.217A>G) pathogenic?

ERCC4 p.Ile73Val (c.217A>G) is classified Uncertain significance in ERCC4 (ClinVar, Multiple submitters, 7 submitters; last evaluated 2024-07-25). AlphaMissense: likely benign (0.105); Ultra-rare (popmax 0.0384%, nfe); Associated with Inborn genetic diseases.

What condition is associated with ERCC4 p.Ile73Val (c.217A>G)?

ERCC4 p.Ile73Val (c.217A>G) is associated with Inborn genetic diseases, xeroderma pigmentosum group F, XFE progeroid syndrome (ClinVar).

How common is ERCC4 p.Ile73Val (c.217A>G) in the general population?

ERCC4 p.Ile73Val (c.217A>G) is ultra-rare (popmax 0.0384%, nfe) (gnomAD).

What do computational predictors say about ERCC4 p.Ile73Val (c.217A>G)?

AlphaMissense predicts likely benign (score 0.105) — an in-silico prediction, not a clinical call.

ERCC4 p.Ile73Val

c.217A>G · rs141591400 · VCV134143

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 7 submitters

AlphaMissense

likely benign

0.105 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0384%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.105	likely benign
REVEL	0.118	moderately benign-leaning
SaProt	LLR -7.28	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 9.3	GERP 1.4, phastCons 1
Regional constraint	o/e 1.08	unconstrained · MANE · 28 kb · p 0.011 · regional, not allelic
Overall
CADD	20.7	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

Grpmax group 0.0384% European (non-Finnish) · 453/1,179,196 alleles

Filtering AF 0.0355% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0343%

Overall 0.0318% 513/1,613,224 alleles · ultra-rare

Ancestry group	Frequency	1 in
Remaining individualsnot grpmax-eligible	0.0464%	2,154
European (non-Finnish)grpmax	0.0384%	2,603
Admixed American	0.0317%	3,159
Middle Eastern	0.0165%	6,062
African / African-American	0.012%	8,338
Finnishnot grpmax-eligible	0.00156%	64,012
South Asian	0.0011%	91,056

Remaining individuals shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.

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: ERCC4
Protein: p.Ile73Val
Coding: c.217A>G
MANE Select: NM_005236
dbSNP: rs141591400
Type: single nucleotide variant
Location: chr16:13922040 (GRCh38)
Gene constraint: LOEUF 0.984 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 74.60 · 13 PDB
Residue 73: the 'helicase-like' region

Full ERCC4 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

Also linked: xeroderma pigmentosum group F XFE progeroid syndrome Fanconi anemia complementation group Q Cockayne syndrome

Similar variants

ERCC4 p.Ile73= Likely benign ★ same residue
ERCC4 c.1102+1G>T Likely pathogenic ★★ same condition
ERCC4 c.793-2A>G Pathogenic ★★ same condition
ERCC4 p.Arg20Ter Pathogenic ★★ same condition
ERCC4 p.Arg589Trp Pathogenic/Likely pathogenic ★★ same condition
ERCC4 p.Arg689Ser Likely pathogenic ★★ same condition
ERCC4 p.Arg772Ter Pathogenic/Likely pathogenic ★★ same condition
ERCC4 p.Cys236Arg 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/ercc4-p-ile73val (accessed [today's date]).

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