Is BMPR1A p.Asp70= (c.210T>C) pathogenic?

BMPR1A p.Asp70= (c.210T>C) is classified Benign/Likely benign in BMPR1A (ClinVar, Multiple submitters, 4 submitters; last evaluated 2025-01-05). No allele count reported in gnomAD v4.1 (AN 1,614,162); Associated with hereditary neoplastic syndrome.

What condition is associated with BMPR1A p.Asp70= (c.210T>C)?

BMPR1A p.Asp70= (c.210T>C) is associated with hereditary neoplastic syndrome, juvenile polyposis syndrome (ClinVar).

How common is BMPR1A p.Asp70= (c.210T>C) in the general population?

BMPR1A p.Asp70= (c.210T>C) is no allele count reported in gnomAD v4.1 (AN 1,614,162) (gnomAD).

BMPR1A p.Asp70=

c.210T>C · rs1589763468 · VCV762171

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

gnomAD v4.1

Not reported

no allele count reported in gnomAD v4.1 (AN 1,614,162)

Conditions

hereditary neoplastic syndrome

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 0.48	GERP -2.3, phastCons 1
Overall
CADD	8.662	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

No allele count reported in gnomAD v4.1 (AN 1,614,162). 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: BMPR1A
Protein: p.Asp70=
Coding: c.210T>C
MANE Select: NM_004329
dbSNP: rs1589763468
Type: single nucleotide variant
Location: chr10:86890204 (GRCh38)
Gene constraint: LOEUF 0.195 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 82.86 · 11 PDB

Full BMPR1A gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

hereditary neoplastic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: juvenile polyposis syndrome

Similar variants

BMPR1A p.Asp70Asn Uncertain significance ★★ ⚠ same residue
BMPR1A p.Asp70Glu Uncertain significance ★★ ⚠ same residue
BMPR1A p.Asp70Val Uncertain significance ★★ ⚠ same residue
BMPR1A p.Asp70Gly Uncertain significance ★ ⚠ same residue
BMPR1A c.1166+1G>A Likely pathogenic ★★ same condition
BMPR1A c.1343-2A>G Likely pathogenic ★★ same condition
BMPR1A c.1473+1G>A Pathogenic/Likely pathogenic ★★ same condition
BMPR1A c.1473+1G>C Pathogenic/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/bmpr1a-p-asp70 (accessed [today's date]).

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