Is EYS p.Ser1927Pro (c.5779T>C) pathogenic?

EYS p.Ser1927Pro (c.5779T>C) is classified Uncertain significance in EYS (ClinVar, Single submitter, 2 submitters; last evaluated 2022-07-23). AlphaMissense: likely benign (0.106); Ultra-rare (popmax 0.0101%, amr); Associated with retinitis pigmentosa 25.

What condition is associated with EYS p.Ser1927Pro (c.5779T>C)?

EYS p.Ser1927Pro (c.5779T>C) is associated with retinitis pigmentosa 25 (ClinVar).

How common is EYS p.Ser1927Pro (c.5779T>C) in the general population?

EYS p.Ser1927Pro (c.5779T>C) is ultra-rare (popmax 0.0101%, amr) (gnomAD).

How is Retinitis pigmentosa inherited?

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

What do computational predictors say about EYS p.Ser1927Pro (c.5779T>C)?

AlphaMissense predicts likely benign (score 0.106) — an in-silico prediction, not a clinical call.

EYS p.Ser1927Pro

c.5779T>C · rs921629471 · VCV1022645

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.106 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0101%, amr)

Missense predictors

0/2 damaging

AlphaMissense, REVEL · SaProt no call

Conditions

retinitis pigmentosa 25

Computational evidence

Protein change
AlphaMissense	0.106	likely benign
REVEL	0.218	benign-leaning
SaProt	—	not scored · why
⇒ AlphaMissense and REVEL both call this tolerated; SaProt makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 4.1	GERP 1.4, phastCons 0.97
Regional constraint	o/e 1.08	unconstrained · MANE · 1,775 kb · p 4.6e-07 · regional, not allelic
Overall
CADD	16.02	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 is an independent agreement signal.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0101% Admixed American · 4/39,668 alleles

Filtering AF 0.00335% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00198%

Overall 0.000405% 6/1,482,664 alleles · ultra-rare exomes 4/1,330,860 · genomes 2/151,804 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.0101%	9,917
European (non-Finnish)	0.000179%	558,425

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: EYS
Protein: p.Ser1927Pro
Coding: c.5779T>C
MANE Select: NM_001142800
dbSNP: rs921629471
Type: single nucleotide variant
Location: chr6:64439218 (GRCh38)
Gene constraint: LOEUF 0.96 · pLI <0.01 (gnomAD)
Residue 1927: the laminin g-like 1 domain

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

Disease context

retinitis pigmentosa 25 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Retinitis pigmentosa (Orphanet):

Inheritance: Autosomal dominant, Autosomal recessive, Mitochondrial inheritance
Onset: Adolescent, Adult, Childhood
Prevalence: 1-5 / 10 000 (Europe)

Similar variants

EYS p.Ser1927Ter Likely pathogenic ★ same residue
EYS p.Ser1927= Likely benign ★ same residue
EYS c.1056+1G>A Pathogenic/Likely pathogenic ★★ same condition
EYS c.1056+3A>C Likely pathogenic ★★ same condition
EYS c.1057-1G>A Likely pathogenic ★★ same condition
EYS c.1184+1G>A Pathogenic/Likely pathogenic ★★ same condition
EYS c.1184+1G>T Likely pathogenic ★★ same condition
EYS c.1185-1G>A Likely 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/eys-p-ser1927pro (accessed [today's date]).

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