Is ABCC2 p.Val1197fs (c.3589_3590del) pathogenic?

ABCC2 p.Val1197fs (c.35893590del) is classified Pathogenic in ABCC2 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-02-25). Very rare (popmax 8.47e-05%, nfe).

How common is ABCC2 p.Val1197fs (c.3589_3590del) in the general population?

ABCC2 p.Val1197fs (c.3589_3590del) is very rare (popmax 8.47e-05%, nfe) (gnomAD).

ABCC2 p.Val1197fs

c.3589_3590del · rs2038821887 · VCV2867633

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

Consequence

frameshift

predicted LoF

gnomAD v4.1

Rare

very rare (popmax 8.47e-05%, nfe)

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	frameshift	predicted loss-of-function
NMD	predicted	premature termination codon in exon 25 of 32
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 1.9	GERP -1.8, phastCons 1

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 8.47e-05% European (non-Finnish) · 1/1,180,016 alleles

Overall 6.84e-05% 1/1,461,888 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: ABCC2
Protein: p.Val1197fs
Coding: c.3589_3590del
MANE Select: NM_000392
dbSNP: rs2038821887
Type: Microsatellite
Location: chr10:99836262 (GRCh38)
Gene constraint: LOEUF 0.985 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 81.40 · 16 PDB
Residue 1197: an α-helix; the abc transmembrane type-1 2 domain

Full ABCC2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

ABCC2 p.Val1197= Conflicting classifications of pathogenicity ★ same residue
ABCC2 p.Glu1405del Uncertain significance ★★ same type
ABCC2 p.Ala364fs Pathogenic ★ same type
ABCC2 p.Ile799fs Pathogenic ★ same type
ABCC2 p.Thr912_Leu913insTer Pathogenic ★ same type
ABCC2 p.Tyr776fs Pathogenic ★ same type
ABCC2 c.2620+10_2620+12del Conflicting classifications of pathogenicity ★ same type
ABCC2 p.Ile1380_Pro1381insIle Uncertain significance ★ same type

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-val1197fs (accessed [today's date]).

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