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CFAP298 p.Ala179=

c.537A>G · rs1601151318 · VCV740557

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation/SpliceAI carries the signal.
REVEL0.17moderately benign-leaning
Splicing
SpliceAIΔ0.68acceptor loss · deltas
Constraint at this position
ConservationphyloP -2.6GERP -0.92
Overall
CADD2.033PHRED · no single calibrated threshold — expert panels disagree

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
CFAP298
Protein
p.Ala179=
Coding
c.537A>G
MANE Select
NM_021254
dbSNP
rs1601151318
Type
single nucleotide variant
Location
chr21:32603290 (GRCh38)
Gene constraint
LOEUF 1.267 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 86.54
Full CFAP298 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/cfap298-p-ala179 (accessed [today's date]).

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