Send feedback

CARD8 p.Glu8Asp

c.24A>T · rs2146671147 · VCV1365014

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 carries the signal.
REVEL0.106moderately benign-leaning
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP -0.47GERP -0.58
Regional constrainto/e 0.86unconstrained · MANE · 29 kb · p 0.00022 · regional, not allelic
Overall
CADD12.47PHRED · 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
CARD8
Protein
p.Glu8Asp
Coding
c.24A>T
MANE Select
NM_001184900
dbSNP
rs2146671147
Type
single nucleotide variant
Location
chr19:48240997 (GRCh38)
Gene constraint
LOEUF 0.883 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 71.42 · 5 PDB
Residue 8
the 'disordered' region
Full CARD8 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/card8-p-glu8asp (accessed [today's date]).

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