Is CREBBP p.Pro1890= (c.5670C>T) pathogenic?

CREBBP p.Pro1890= (c.5670C>T) is classified Benign in CREBBP (ClinVar, Multiple submitters, 5 submitters; last evaluated 2026-02-02). Low-frequency (popmax 4.94%, afr); Associated with Rubinstein-Taybi syndrome.

What condition is associated with CREBBP p.Pro1890= (c.5670C>T)?

CREBBP p.Pro1890= (c.5670C>T) is associated with Rubinstein-Taybi syndrome (ClinVar).

How common is CREBBP p.Pro1890= (c.5670C>T) in the general population?

CREBBP p.Pro1890= (c.5670C>T) is low-frequency (popmax 4.94%, afr) (gnomAD).

CREBBP p.Pro1890=

c.5670C>T · rs115594471 · VCV288743

Benign Multiple submitters

Classification

Benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 5 submitters

gnomAD v4.1

Rare

low-frequency (popmax 4.94%, afr)

Conditions

Rubinstein-Taybi syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP -2.9	GERP -3.8
Overall
CADD	4.523	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 4.94% African / African-American · 3,706/74,988 alleles

Filtering AF 4.81% ClinGen BA1/BS1 input FAF95, joint · FAF99 4.76%

Overall 0.31% 4,994/1,609,474 alleles · low-frequency

Ancestry group	Frequency	1 in
African / African-Americangrpmax	4.94%	20
Middle Eastern	0.759%	132
Admixed American	0.654%	153
Remaining individualsnot grpmax-eligible	0.492%	203
Ashkenazi Jewishnot grpmax-eligible	0.406%	246
European (non-Finnish)	0.0349%	2,863
South Asian	0.00989%	10,116
Finnishnot grpmax-eligible	0.00333%	30,016

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: CREBBP
Protein: p.Pro1890=
Coding: c.5670C>T
MANE Select: NM_004380
dbSNP: rs115594471
Type: single nucleotide variant
Location: chr16:3729377 (GRCh38)
Gene constraint: LOEUF 0.101 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 54.31 · 144 PDB
Residue 1890: the 'interaction with trerf1' region; the 'disordered' region

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

Disease context

Rubinstein-Taybi syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CREBBP c.2881-13G>A Pathogenic/Likely pathogenic ★★ same condition
CREBBP c.3779+1G>A Pathogenic ★★ same condition
CREBBP c.3779+1G>T Pathogenic ★★ same condition
CREBBP c.3836+1G>A Pathogenic ★★ same condition
CREBBP p.Arg1103Ter Pathogenic ★★ same condition
CREBBP p.Arg1233Lys Pathogenic/Likely pathogenic ★★ ⚠ same condition
CREBBP p.Arg1498Ter Pathogenic ★★ same condition
CREBBP p.Arg1867Gln Pathogenic/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/crebbp-p-pro1890 (accessed [today's date]).

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