Is ARSL p.Asp72= (c.216C>T) pathogenic?

ARSL p.Asp72= (c.216C>T) is classified Benign/Likely benign in ARSL (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-11-10). Rare (popmax 0.121%, eas); Associated with chondrodysplasia punctata, brachytelephalangic, autosomal.

What condition is associated with ARSL p.Asp72= (c.216C>T)?

ARSL p.Asp72= (c.216C>T) is associated with chondrodysplasia punctata, brachytelephalangic, autosomal (ClinVar).

How common is ARSL p.Asp72= (c.216C>T) in the general population?

ARSL p.Asp72= (c.216C>T) is rare (popmax 0.121%, eas) (gnomAD).

ARSL p.Asp72=

c.216C>T · rs767307974 · VCV1683204

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

rare (popmax 0.121%, eas)

Conditions

chondrodysplasia punctata, brachytelephalangic, autosomal

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 -20	GERP -2.7
Overall
CADD	0.008	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.121% East Asian · 41/33,751 alleles

Filtering AF 0.092% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0817%

Overall 0.00513% 62/1,209,343 alleles · rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.121%	823
Finnishnot grpmax-eligible	0.0172%	5,817
Remaining individualsnot grpmax-eligible	0.0168%	5,949
South Asian	0.0053%	18,885
African / African-American	0.00175%	57,247
European (non-Finnish)	0.000112%	894,839

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: ARSL
Protein: p.Asp72=
Coding: c.216C>T
MANE Select: NM_000047
dbSNP: rs767307974
Type: single nucleotide variant
Location: chrX:2955507 (GRCh38)
Structure: AlphaFold pLDDT 92.57

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

Disease context

chondrodysplasia punctata, brachytelephalangic, autosomal — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

ARSL c.24-2A>G Likely pathogenic ★★ same condition
ARSL p.Gly73Ser Likely pathogenic ★★ ⚠ same condition
ARSL p.Ala182Thr Uncertain significance ★★ ⚠ same condition
ARSL p.Ala251Val Uncertain significance ★★ ⚠ same condition
ARSL p.Ala45Val Uncertain significance ★★ ⚠ same condition
ARSL p.Arg12Ser Uncertain significance ★★ ⚠ same condition
ARSL p.Arg190His Uncertain significance ★★ ⚠ same condition
ARSL p.Asp413Glu 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/arsl-p-asp72 (accessed [today's date]).

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