Is CDC73 p.Pro84Thr (c.250C>A) pathogenic?

CDC73 p.Pro84Thr (c.250C>A) is classified Uncertain significance in CDC73 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-03-30). AlphaMissense: ambiguous (0.435); No allele count reported in gnomAD v4.1 (AN 1,587,800); Associated with parathyroid gland carcinoma.

What condition is associated with CDC73 p.Pro84Thr (c.250C>A)?

CDC73 p.Pro84Thr (c.250C>A) is associated with parathyroid gland carcinoma (ClinVar).

How common is CDC73 p.Pro84Thr (c.250C>A) in the general population?

CDC73 p.Pro84Thr (c.250C>A) is no allele count reported in gnomAD v4.1 (AN 1,587,800) (gnomAD).

How is Parathyroid carcinoma inherited?

Typically Not applicable (Orphanet). A genetic counselor can assess individual risk for a family.

What do computational predictors say about CDC73 p.Pro84Thr (c.250C>A)?

AlphaMissense predicts ambiguous (score 0.435) — an in-silico prediction, not a clinical call.

CDC73 p.Pro84Thr

c.250C>A · VCV3648166

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.435 · ACMG-weighted

gnomAD v4.1

Not reported

no allele count reported in gnomAD v4.1 (AN 1,587,800)

Missense predictors

2/2 damaging

REVEL, SaProt · AlphaMissense no call

Conditions

parathyroid gland carcinoma

Computational evidence

Protein change
AlphaMissense	0.435	ambiguous
REVEL	0.709	pathogenic-leaning
SaProt	LLR -11.77	damaging
⇒ REVEL and SaProt both call this damaging; AlphaMissense makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 4.9	GERP 1.9, phastCons 1
Regional constraint	o/e 0.57	unconstrained · MANE · 16 kb · p 1.1e-08 · regional, not allelic
Overall
CADD	25.8	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

No allele count reported in gnomAD v4.1 (AN 1,587,800). This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.

Variant & gene context

Gene: CDC73
Protein: p.Pro84Thr
Coding: c.250C>A
MANE Select: NM_024529
Type: single nucleotide variant
Location: chr1:193130186 (GRCh38)
Gene constraint: LOEUF 0.42 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 73.94 · 21 PDB
Residue 84: an α-helix

Full CDC73 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

parathyroid gland carcinoma — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Parathyroid carcinoma (Orphanet):

Inheritance: Not applicable
Onset: Adult
Prevalence: <1 / 1 000 000 (Europe)

Similar variants

CDC73 p.Pro84= Conflicting classifications of pathogenicity ★ same residue
CDC73 p.Pro84Ser Uncertain significance ★ ⚠ same residue
CDC73 p.Pro84Ala Uncertain significance ★ ⚠ same residue
CDC73 c.1030+2T>C Likely pathogenic ★★ same condition
CDC73 c.131+1G>A Pathogenic/Likely pathogenic ★★ same condition
CDC73 c.237+1G>A Pathogenic ★★ same condition
CDC73 c.423+1G>A Pathogenic ★★ same condition
CDC73 c.513-1G>A 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/cdc73-p-pro84thr (accessed [today's date]).

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