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CDK13 p.Gly1032=

c.3096C>T · rs2484054811 · VCV2446278

Uncertain significance Single submitter
Classification
Uncertain significance
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.
Splicing
SpliceAIΔ0.28donor gain · deltas
Constraint at this position
ConservationphyloP 1.5GERP -0.37, phastCons 1
Overall
CADD15.66PHRED · 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
CDK13
Protein
p.Gly1032=
Coding
c.3096C>T
MANE Select
NM_003718
dbSNP
rs2484054811
Type
single nucleotide variant
Location
chr7:40088192 (GRCh38)
Gene constraint
LOEUF 0.434 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure
AlphaFold pLDDT 50.59 · 2 PDB
Residue 1032
the 'disordered' region
Full CDK13 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/cdk13-p-gly1032 (accessed [today's date]).

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