Is ACD p.Pro256= (c.768G>A) pathogenic?

ACD p.Pro256= (c.768G>A) is classified Likely benign in ACD (ClinVar, Multiple submitters, 3 submitters; last evaluated 2026-03-01). Very rare (popmax 0.00135%, afr); Associated with Inborn genetic diseases.

What condition is associated with ACD p.Pro256= (c.768G>A)?

ACD p.Pro256= (c.768G>A) is associated with Inborn genetic diseases, dyskeratosis congenita, autosomal dominant 6 (ClinVar).

How common is ACD p.Pro256= (c.768G>A) in the general population?

ACD p.Pro256= (c.768G>A) is very rare (popmax 0.00135%, afr) (gnomAD).

ACD p.Pro256=

c.768G>A · rs1245603152 · VCV1694801

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

very rare (popmax 0.00135%, afr)

Conditions

Inborn genetic diseases

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 -9.7	GERP -2.9
Overall
CADD	1.627	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00135% African / African-American · 1/74,006 alleles

Filtering AF 0.000509% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000372%

Overall 0.000761% 12/1,576,278 alleles · very rare exomes 12/1,424,152 · genomes 0/152,126 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.00135%	74,006
European (non-Finnish)	0.000948%	105,441

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: ACD
Protein: p.Pro256=
Coding: c.768G>A
MANE Select: NM_001082486
dbSNP: rs1245603152
Type: single nucleotide variant
Location: chr16:67658616 (GRCh38)
Gene constraint: LOEUF 0.921 · pLI <0.01 · ClinGen HI 0/3 (gnomAD)
Structure: AlphaFold pLDDT 63.09 · 28 PDB

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

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: dyskeratosis congenita, autosomal dominant 6

Similar variants

ACD p.Pro256Leu Uncertain significance ★★ ⚠ same residue
ACD p.Pro256Arg Uncertain significance ★ ⚠ same residue
ACD c.645+2T>C Uncertain significance ★★ same condition
ACD c.99+5G>A Uncertain significance ★★ same condition
ACD c.-20C>T Uncertain significance ★★ same condition
ACD c.-24C>T Uncertain significance ★★ same condition
ACD c.-26T>G Uncertain significance ★★ same condition
ACD c.-29C>A Uncertain significance ★★ 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/acd-p-pro256 (accessed [today's date]).

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