Is MFRP p.Arg64= (c.192C>T) pathogenic?

MFRP p.Arg64= (c.192C>T) is classified Likely benign in MFRP (ClinVar, Single submitter, 1 submitter; last evaluated 2022-06-13). Very rare (popmax 8.51e-05%, nfe); Associated with isolated microphthalmia 5.

What condition is associated with MFRP p.Arg64= (c.192C>T)?

MFRP p.Arg64= (c.192C>T) is associated with isolated microphthalmia 5 (ClinVar).

How common is MFRP p.Arg64= (c.192C>T) in the general population?

MFRP p.Arg64= (c.192C>T) is very rare (popmax 8.51e-05%, nfe) (gnomAD).

MFRP p.Arg64=

Q: How is Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome inherited?

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

c.192C>T · rs200143181 · VCV1555786

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 8.51e-05%, nfe)

Conditions

isolated microphthalmia 5

⚠ Built without this gene's context — gene constraint and dosage, protein structure, pathways, panels and related-variant links were not looked up for this page. why

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not looked up on this page · why
Constraint at this position
Conservation	phyloP 0.069	GERP -2.7
Overall
CADD	6.715	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 8.51e-05% European (non-Finnish) · 1/1,175,092 alleles

Overall 6.23e-05% 1/1,603,890 alleles · very rare exomes 1/1,451,620 · genomes 0/152,270 · 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: MFRP
Protein: p.Arg64=
Coding: c.192C>T
MANE Select: NM_031433
dbSNP: rs200143181
Type: single nucleotide variant
Location: chr11:119346125 (GRCh38)

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

Disease context

isolated microphthalmia 5 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome (Orphanet):

Inheritance: Autosomal recessive
Onset: Adult

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/mfrp-p-arg64 (accessed [today's date]).

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