Is BIN3 p.Asp192Tyr (c.574G>T) pathogenic?

BIN3 p.Asp192Tyr (c.574G>T) is classified Uncertain significance in BIN3 (ClinVar, Single submitter, 1 submitter; last evaluated 2023-05-04). AlphaMissense: ambiguous (0.4517); Ultra-rare (popmax 0.0534%, afr).

How common is BIN3 p.Asp192Tyr (c.574G>T) in the general population?

BIN3 p.Asp192Tyr (c.574G>T) is ultra-rare (popmax 0.0534%, afr) (gnomAD).

What do computational predictors say about BIN3 p.Asp192Tyr (c.574G>T)?

AlphaMissense predicts ambiguous (score 0.4517) — an in-silico prediction, not a clinical call.

BIN3 p.Asp192Tyr

c.574G>T · rs201431458 · VCV2561198

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4517 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0534%, afr)

Computational evidence

Protein change
AlphaMissense	0.4517	ambiguous
REVEL	0.383	indeterminate
SaProt	LLR -10.90	damaging
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 2.7	GERP -1.3, phastCons 0.99
Regional constraint	o/e 1.11	unconstrained · MANE · 48 kb · p 0.041 · regional, not allelic
Overall
CADD	24.3	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0534% African / African-American · 40/74,886 alleles

Filtering AF 0.0402% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0357%

Overall 0.00279% 45/1,611,048 alleles · ultra-rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.0534%	1,872
Remaining individualsnot grpmax-eligible	0.00642%	15,574
Admixed American	0.00167%	59,856

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: BIN3
Protein: p.Asp192Tyr
Coding: c.574G>T
MANE Select: NM_018688
dbSNP: rs201431458
Type: single nucleotide variant
Location: chr8:22623956 (GRCh38)
Gene constraint: LOEUF 1.45 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 92.83
Residue 192: the bar domain

Full BIN3 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

BIN3 p.Asp192Glu Uncertain significance ★ ⚠ same residue
BIN3 c.297+5C>T Benign ★★ same type
BIN3 p.Ala131Pro Uncertain significance ★ ⚠ same type
BIN3 p.Arg128Gln Uncertain significance ★ ⚠ same type
BIN3 p.Arg128Trp Uncertain significance ★ ⚠ same type
BIN3 p.Arg136Gly Uncertain significance ★ ⚠ same type
BIN3 p.Arg166Gln Uncertain significance ★ ⚠ same type
BIN3 p.Arg185Cys 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/bin3-p-asp192tyr (accessed [today's date]).

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