Is APC p.Asp2016Tyr (c.6046G>T) pathogenic?

APC p.Asp2016Tyr (c.6046G>T) is classified Uncertain significance in APC (ClinVar, Single submitter, 1 submitter; last evaluated 2018-08-01). AlphaMissense: likely pathogenic (0.8856); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with APC p.Asp2016Tyr (c.6046G>T)?

APC p.Asp2016Tyr (c.6046G>T) is associated with hereditary neoplastic syndrome (ClinVar).

How common is APC p.Asp2016Tyr (c.6046G>T) in the general population?

APC p.Asp2016Tyr (c.6046G>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about APC p.Asp2016Tyr (c.6046G>T)?

AlphaMissense predicts likely pathogenic (score 0.8856) — an in-silico prediction, not a clinical call.

APC p.Asp2016Tyr

c.6046G>T · rs1561604731 · VCV584480

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.8856 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

2/2 damaging

AlphaMissense, REVEL · SaProt no call

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.8856	likely pathogenic
REVEL	0.752	pathogenic-leaning
SaProt	—	not scored · why
⇒ AlphaMissense and REVEL both call this damaging; SaProt makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 12	GERP 2.8, phastCons 1
Regional constraint	o/e 1.08	unconstrained · MANE · 4,236 bp · p 0.00065 · regional, not allelic
Overall
CADD	28.3	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean damaging — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL is an independent agreement signal.

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.Asp2016Tyr
Coding: c.6046G>T
MANE Select: NM_000038
dbSNP: rs1561604731
Type: single nucleotide variant
Location: chr5:112841640 (GRCh38)
Gene constraint: LOEUF 0.321 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)

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.Asp2016Val Uncertain significance ★★ ⚠ same residue
APC p.Asp2016Gly Uncertain significance ★ ⚠ same residue
APC p.Asp2016= Benign/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
APC c.1312+5G>C Likely pathogenic ★★★ same condition
APC c.1409-3T>G 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-asp2016tyr (accessed [today's date]).

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