Is RPGR p.Ala366= (c.1098T>C) pathogenic?

RPGR p.Ala366= (c.1098T>C) is classified Benign in RPGR (ClinVar, Single submitter, 3 submitters; last evaluated 2026-01-21). Very rare (popmax 0.00715%, nfe); Associated with primary ciliary dyskinesia.

What condition is associated with RPGR p.Ala366= (c.1098T>C)?

RPGR p.Ala366= (c.1098T>C) is associated with primary ciliary dyskinesia (ClinVar).

How common is RPGR p.Ala366= (c.1098T>C) in the general population?

RPGR p.Ala366= (c.1098T>C) is very rare (popmax 0.00715%, nfe) (gnomAD).

How is Primary ciliary dyskinesia inherited?

Typically Autosomal dominant, Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

RPGR p.Ala366=

c.1098T>C · rs369391462 · VCV697500

Benign Single submitter

Classification

Benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

very rare (popmax 0.00715%, nfe)

Conditions

primary ciliary dyskinesia

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
REVEL	0.033	moderately benign-leaning
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 5.2	GERP -0.52, phastCons 1
Overall
CADD	7.183	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00715% European (non-Finnish) · 64/895,170 alleles

Filtering AF 0.00573% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00521%

Overall 0.00529% 64/1,209,903 alleles · very rare exomes 56/1,097,761 · genomes 8/112,142 · joint denominator

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: RPGR
Protein: p.Ala366=
Coding: c.1098T>C
MANE Select: NM_001034853
dbSNP: rs369391462
Type: single nucleotide variant
Location: chrX:38299103 (GRCh38)
Structure: AlphaFold pLDDT 56.59 · 3 PDB
Residue 366: a β-strand

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

Disease context

primary ciliary dyskinesia — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Primary ciliary dyskinesia (Orphanet):

Inheritance: Autosomal dominant, Autosomal recessive, X-linked recessive
Onset: Neonatal
Prevalence: 1-5 / 10 000 (Pakistan)

Similar variants

RPGR c.1245+3A>G Pathogenic ★★★ same condition
RPGR c.1572+1G>A Pathogenic ★★★ same condition
RPGR c.1573-1G>A Pathogenic ★★★ same condition
RPGR c.1573-8A>G Likely pathogenic ★★★ same condition
RPGR c.1754-3C>G Pathogenic ★★★ same condition
RPGR c.247+5G>A Pathogenic ★★★ same condition
RPGR c.310+1G>C Pathogenic ★★★ same condition
RPGR c.310+3A>G 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/rpgr-p-ala366 (accessed [today's date]).

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