Is APC p.Arg1920Ter (c.5758C>T) pathogenic?

APC p.Arg1920Ter (c.5758C>T) is classified Pathogenic/Likely pathogenic in APC (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-06-17). Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with APC p.Arg1920Ter (c.5758C>T)?

APC p.Arg1920Ter (c.5758C>T) is associated with hereditary neoplastic syndrome (ClinVar).

How common is APC p.Arg1920Ter (c.5758C>T) in the general population?

APC p.Arg1920Ter (c.5758C>T) is absent from gnomAD v4.1 (gnomAD).

APC p.Arg1920Ter

c.5758C>T · rs587779800 · VCV1691813

Pathogenic/Likely pathogenic Multiple submitters

Classification

Pathogenic/Likely pathogenic

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

Consequence

nonsense (stop-gain)

predicted LoF

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	nonsense (stop-gain)	predicted loss-of-function in a haploinsufficient gene (ClinGen)
NMD	escapes	premature termination codon in the last exon (16 of 16) — the truncated protein is likely expressed. PVS1 input, not an applied code
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.83	GERP -0.86, phastCons 0.13
Overall
CADD	35.0	PHRED · no single calibrated threshold — expert panels disagree

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

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: APC
Protein: p.Arg1920Ter
Coding: c.5758C>T
MANE Select: NM_000038 · reported on NM_001127510
dbSNP: rs587779800
Type: single nucleotide variant
Location: chr5:112841352 (GRCh38)
Gene constraint: LOEUF 0.321 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Residue 1920: the 'disordered' region

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

Disease context

hereditary neoplastic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

APC p.Arg1920Gln Uncertain significance ★★ ⚠ same residue
APC p.Arg1920Leu Uncertain significance ★★ same residue
APC p.Arg1920Gly Conflicting classifications of pathogenicity ★ same residue
APC p.Arg1920fs Pathogenic ★★ same residue
APC p.Arg1920= Likely benign ★ same residue
APC c.1312+3A>C Likely pathogenic ★★★ same condition
APC c.1312+3A>G Pathogenic ★★★ same condition
APC c.1312+5G>A Likely pathogenic ★★★ same condition

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/apc-p-arg1920ter (accessed [today's date]).

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