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EVC p.Gln74Pro

c.221_222delinsCA · rs2474374652 · VCV2018850

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Not reported
no gnomAD frequency available for this variant
Conditions
2
Ellis-van Creveld syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 2GERP -0.74, phastCons 1
Regional constrainto/e 1.12unconstrained · MANE · 100 kb · p 1.2e-05 · regional, not allelic

Population frequency

dbSNP / gnomAD

No gnomAD frequency available for this variant. This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.

Variant & gene context

Gene
EVC
Protein
p.Gln74Pro
Coding
c.221_222delinsCA
MANE Select
NM_153717
dbSNP
rs2474374652
Type
Indel
Location
chr4:5719294 (GRCh38)
Gene constraint
LOEUF 1.134 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 74.49
Residue 74
a UniProt-annotated variant site (in); the 'disordered' region
Full EVC gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/evc-p-gln74pro (accessed [today's date]).

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