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CACNA1E p.Arg360fs

c.1078_1081del · rs147596634 · VCV2859942

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Not reported
no allele count reported in gnomAD v4.1 (AN 1,553,606)

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequenceframeshiftpredicted loss-of-function in a LoF-intolerant gene
NMDpredictedpremature termination codon in exon 8 of 48
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 11GERP 2.3, phastCons 1

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Population frequency

gnomAD v4.1 · exomes + genomes

No allele count reported in gnomAD v4.1 (AN 1,553,606). 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
CACNA1E
Protein
p.Arg360fs
Coding
c.1078_1081del
MANE Select
NM_001205293
dbSNP
rs147596634
Type
Microsatellite
Location
chr1:181710966 (GRCh38)
Gene constraint
LOEUF 0.221 · pLI 1.00 · ClinGen HI 1/3 (gnomAD)
Structure
AlphaFold pLDDT 60.56 · 5 PDB
Full CACNA1E 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/cacna1e-p-arg360fs (accessed [today's date]).

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