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CEP152 c.1908+10A>T

rs1466501710 · VCV2792954

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 carries the signal.
Splicing
Splice regiondonor +10near-intronic (+10 nt from the splice site)
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP 0.12GERP -1.3
Non-coding constraintZ 0.521 kb window · o/e 0.96 · regional · uncalibrated
Overall
CADD3.218PHRED · 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
CEP152
Coding
c.1908+10A>T
MANE Select
NM_001194998
dbSNP
rs1466501710
Type
single nucleotide variant
Location
chr15:48768946 (GRCh38)
Gene constraint
LOEUF 0.784 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 61.54 · 3 PDB
Full CEP152 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/cep152-c-1908-plus-10a-t (accessed [today's date]).

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