Is RBP1 p.Pro51= (c.153G>A) pathogenic?

RBP1 p.Pro51= (c.153G>A) is classified Likely benign in RBP1 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-05-24). Very rare (popmax 0.00515%, amr).

How common is RBP1 p.Pro51= (c.153G>A) in the general population?

RBP1 p.Pro51= (c.153G>A) is very rare (popmax 0.00515%, amr) (gnomAD).

RBP1 p.Pro51=

c.153G>A · rs1160288200 · VCV1926989

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00515%, amr)

⚠ 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 0.13	GERP -2.3
Overall
CADD	11.05	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00515% Admixed American · 3/58,226 alleles

Filtering AF 0.00137% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000679%

Overall 0.00025% 4/1,598,378 alleles · very rare exomes 4/1,446,064 · genomes 0/152,314 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.00515%	19,409
Remaining individualsnot grpmax-eligible	0.00162%	61,806

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: RBP1
Protein: p.Pro51=
Coding: c.153G>A
MANE Select: NM_002899
dbSNP: rs1160288200
Type: single nucleotide variant
Location: chr3:139539566 (GRCh38)

Full RBP1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

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/rbp1-p-pro51 (accessed [today's date]).

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