Is HGD p.Asp124= (c.372C>T) pathogenic?

HGD p.Asp124= (c.372C>T) is classified Benign in HGD (ClinVar, Multiple submitters, 4 submitters; last evaluated 2026-01-31). Low-frequency (popmax 3.73%, mid); Associated with alkaptonuria.

What condition is associated with HGD p.Asp124= (c.372C>T)?

HGD p.Asp124= (c.372C>T) is associated with alkaptonuria (ClinVar).

How common is HGD p.Asp124= (c.372C>T) in the general population?

HGD p.Asp124= (c.372C>T) is low-frequency (popmax 3.73%, mid) (gnomAD).

How is Alkaptonuria inherited?

Typically Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

HGD p.Asp124=

c.372C>T · rs140977117 · VCV342749

Benign Multiple submitters

Classification

Benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

gnomAD v4.1

Rare

low-frequency (popmax 3.73%, mid)

Conditions

alkaptonuria

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 2.2	GERP 0.015, phastCons 1
Overall
CADD	8.529	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 3.73% Middle Eastern · 226/6,060 alleles

Filtering AF 3.33% ClinGen BA1/BS1 input FAF95, joint · FAF99 3.18%

Overall 2.4% 38,722/1,613,576 alleles · low-frequency

Ancestry group	Frequency	1 in
Finnishnot grpmax-eligible	4.82%	21
Middle Easterngrpmax	3.73%	27
Ashkenazi Jewishnot grpmax-eligible	3.6%	28
Amishnot grpmax-eligible	3.08%	33
European (non-Finnish)	2.59%	39
Remaining individualsnot grpmax-eligible	2.51%	40
South Asian	1.32%	76
Admixed American	1.29%	77
African / African-American	0.354%	282
East Asian	0.0201%	4,986

Finnish shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.

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: HGD
Protein: p.Asp124=
Coding: c.372C>T
MANE Select: NM_000187
dbSNP: rs140977117
Type: single nucleotide variant
Location: chr3:120650836 (GRCh38)
Gene constraint: LOEUF 1.199 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 96.85 · 2 PDB

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

Disease context

alkaptonuria — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Alkaptonuria (Orphanet):

Inheritance: Autosomal recessive
Onset: Adult, Infancy
Prevalence: 1-9 / 1 000 000 (Worldwide)

Similar variants

HGD c.1007-2A>T Pathogenic ★★ same condition
HGD c.1188+1G>A Pathogenic ★★ same condition
HGD c.15+1G>A Pathogenic/Likely pathogenic ★★ same condition
HGD c.16-1G>A Pathogenic ★★ same condition
HGD c.342+1G>A Pathogenic/Likely pathogenic ★★ same condition
HGD c.342+1G>T Pathogenic ★★ same condition
HGD c.342+3A>C Pathogenic/Likely pathogenic ★★ same condition
HGD c.469+1G>C 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/hgd-p-asp124 (accessed [today's date]).

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