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ABCC2 p.Ile1368=

c.4104T>C · rs2493051474 · VCV2730137

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
SpliceAI<0.2all four deltas below 0.2 · T>A here scores Δ0.37 · evaluated, not missing
Constraint at this position
ConservationphyloP -1.7GERP -5.5
Overall
CADD6.314PHRED · 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
ABCC2
Protein
p.Ile1368=
Coding
c.4104T>C
MANE Select
NM_000392
dbSNP
rs2493051474
Type
single nucleotide variant
Location
chr10:99845740 (GRCh38)
Gene constraint
LOEUF 0.985 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 81.40 · 16 PDB
Residue 1368
the abc transporter 2 domain
Full ABCC2 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/abcc2-p-ile1368 (accessed [today's date]).

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