Is RIGI p.Ser437= (c.1311A>G) pathogenic?

RIGI p.Ser437= (c.1311A>G) is classified Likely benign in RIGI (ClinVar, Single submitter, 1 submitter; last evaluated 2024-06-17). Absent from gnomAD v4.1.

How common is RIGI p.Ser437= (c.1311A>G) in the general population?

RIGI p.Ser437= (c.1311A>G) is absent from gnomAD v4.1 (gnomAD).

RIGI p.Ser437=

c.1311A>G · rs2118801050 · VCV1672255

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Absent

absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP -7.6	GERP -3.9
Overall
CADD	1.067	PHRED · no single calibrated threshold — expert panels disagree

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: RIGI
Protein: p.Ser437=
Coding: c.1311A>G
MANE Select: NM_014314
dbSNP: rs2118801050
Type: single nucleotide variant
Location: chr9:32487535 (GRCh38)
Structure: AlphaFold pLDDT 85.40 · 44 PDB
Residue 437: the 'interaction with zc3hav1' region

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

Similar variants

RIGI p.Ser437Leu Uncertain significance ★★ ⚠ same residue
RIGI c.1923+1G>A Uncertain significance ★★ same type
RIGI c.954-6T>G Uncertain significance ★★ same type
RIGI p.Ala436Val Uncertain significance ★★ ⚠ same type
RIGI p.Ala486Thr Uncertain significance ★★ ⚠ same type
RIGI p.Ala537Ser Uncertain significance ★★ ⚠ same type
RIGI p.Ala537Thr Uncertain significance ★★ ⚠ same type
RIGI p.Ala774Thr 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/rigi-p-ser437 (accessed [today's date]).

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