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CIC c.7186+19C>A

VCV3907488

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00339%, nfe)

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
Splice regiondonor +19near-intronic (+19 nt from the splice site)
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP -2.3GERP -3
Overall
CADD0.374PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes
Grpmax group 0.00339% European (non-Finnish) · 40/1,180,006 alleles
Filtering AF 0.00255% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00225%
Overall 0.00274% 40/1,459,958 alleles · very rare

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene
CIC
Coding
c.7186+19C>A
MANE Select
NM_005984 · reported on NM_001386298
Type
single nucleotide variant
Location
chr19:42294754 (GRCh38)
Structure
AlphaFold pLDDT 75.09
Full CIC 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/cic-c-7186-plus-19c-a (accessed [today's date]).

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