Is SRCAP p.Arg2767Trp (c.8299C>T) pathogenic?

SRCAP p.Arg2767Trp (c.8299C>T) is classified Uncertain significance in SRCAP (ClinVar, Single submitter, 1 submitter; last evaluated 2025-03-07). AlphaMissense: ambiguous (0.4378); Very rare (popmax 0.00182%, amr).

How common is SRCAP p.Arg2767Trp (c.8299C>T) in the general population?

SRCAP p.Arg2767Trp (c.8299C>T) is very rare (popmax 0.00182%, amr) (gnomAD).

What do computational predictors say about SRCAP p.Arg2767Trp (c.8299C>T)?

AlphaMissense predicts ambiguous (score 0.4378) — an in-silico prediction, not a clinical call.

SRCAP p.Arg2767Trp

c.8299C>T · VCV4083160

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4378 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00182%, amr)

Computational evidence

Protein change
AlphaMissense	0.4378	ambiguous
REVEL	0.495	indeterminate
SaProt	—	not scored · why
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 4	GERP 1.3, phastCons 1
Regional constraint	o/e 1.06	unconstrained · MANE · 2,598 bp · p 0.058 · regional, not allelic
Overall
CADD	24.1	PHRED · no single calibrated threshold — expert panels disagree

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00182% Admixed American · 1/54,828 alleles

Filtering AF 0.000365% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000264%

Overall 0.000699% 11/1,574,096 alleles · very rare exomes 9/1,421,890 · genomes 2/152,206 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.00182%	54,828
South Asian	0.00118%	84,950
European (non-Finnish)	0.000776%	128,870

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: SRCAP
Protein: p.Arg2767Trp
Coding: c.8299C>T
MANE Select: NM_006662
Type: single nucleotide variant
Location: chr16:30738339 (GRCh38)
Gene constraint: LOEUF 0.223 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Residue 2767: the 'disordered' region; a UniProt-annotated variant site (in dehmba); a UniProt-annotated variant site (in flhs)

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

Similar variants

SRCAP p.Arg2767Gln Conflicting classifications of pathogenicity ★ same residue
SRCAP p.Arg2329Ter Pathogenic/Likely pathogenic ★★ same type
SRCAP p.Arg2435Ter Pathogenic/Likely pathogenic ★★ same type
SRCAP p.Arg2444Ter Pathogenic ★★ same type
SRCAP p.Arg2718Ter Pathogenic/Likely pathogenic ★★ same type
SRCAP p.Arg2748Ter Pathogenic ★★ same type
SRCAP p.Gln2407Ter Pathogenic ★★ same type
SRCAP p.Gln2419Ter Pathogenic ★★ 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/srcap-p-arg2767trp (accessed [today's date]).

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