Is UBTF p.Asp294= (c.882C>T) pathogenic?

UBTF p.Asp294= (c.882C>T) is classified Likely benign in UBTF (ClinVar, Single submitter, 1 submitter; last evaluated 2022-04-05). Ultra-rare (popmax 0.048%, afr).

How common is UBTF p.Asp294= (c.882C>T) in the general population?

UBTF p.Asp294= (c.882C>T) is ultra-rare (popmax 0.048%, afr) (gnomAD).

UBTF p.Asp294=

c.882C>T · VCV4935400

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

ultra-rare (popmax 0.048%, afr)

⚠ 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 -0.44	GERP -4.5
Overall
CADD	6.778	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.048% African / African-American · 36/75,012 alleles

Filtering AF 0.0356% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0313%

Overall 0.00378% 61/1,613,730 alleles · ultra-rare exomes 36/1,461,530 · genomes 25/152,200 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.048%	2,084
Middle Eastern	0.033%	3,031
Admixed American	0.00666%	15,005
Remaining individualsnot grpmax-eligible	0.0048%	20,837
European (non-Finnish)	0.00127%	78,665
South Asian	0.0011%	91,064

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: UBTF
Protein: p.Asp294=
Coding: c.882C>T
MANE Select: NM_014233
Type: single nucleotide variant
Location: chr17:44211896 (GRCh38)

Full UBTF 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/ubtf-p-asp294 (accessed [today's date]).

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