Is SRGAP1 p.Pro665Ser (c.1993C>T) pathogenic?

SRGAP1 p.Pro665Ser (c.1993C>T) is classified Uncertain significance in SRGAP1 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-07-16). AlphaMissense: likely benign (0.1972); Absent from gnomAD v4.1.

How common is SRGAP1 p.Pro665Ser (c.1993C>T) in the general population?

SRGAP1 p.Pro665Ser (c.1993C>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about SRGAP1 p.Pro665Ser (c.1993C>T)?

AlphaMissense predicts likely benign (score 0.1972) — an in-silico prediction, not a clinical call.

SRGAP1 p.Pro665Ser

c.1993C>T · VCV4174810

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1972 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.1972	likely benign
REVEL	0.229	benign-leaning
SaProt	LLR -8.88	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.7	GERP 1.9, phastCons 1
Regional constraint	o/e 0.80	unconstrained · MANE · 281 kb · p 2.2e-09 · regional, not allelic
Overall
CADD	24.6	PHRED · no single calibrated threshold — expert panels disagree

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

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

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: SRGAP1
Protein: p.Pro665Ser
Coding: c.1993C>T
MANE Select: NM_020762
Type: single nucleotide variant
Location: chr12:64111835 (GRCh38)
Gene constraint: LOEUF 0.47 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 73.49
Residue 665: the rho-gap domain

Full SRGAP1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

SRGAP1 p.Pro665Thr Uncertain significance ★ ⚠ same residue
SRGAP1 p.Arg900Gly Uncertain significance ★★ ⚠ same type
SRGAP1 c.2225-7G>A Likely benign ★★ same type
SRGAP1 p.Asn786= Benign ★★ same type
SRGAP1 p.His875Arg Benign ★★ same type
SRGAP1 p.His924= Benign ★★ same type
SRGAP1 p.Ile371= Benign ★★ same type
SRGAP1 p.Leu49= Benign/Likely benign ★★ 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/srgap1-p-pro665ser (accessed [today's date]).

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