Is DSPP p.Asp1071Val (c.3212A>T) pathogenic?

DSPP p.Asp1071Val (c.3212A>T) is classified Uncertain significance in DSPP (ClinVar, Single submitter, 1 submitter; last evaluated 2024-12-31). AlphaMissense: likely benign (0.3098); Very rare (popmax 8.75e-05%, nfe); Associated with Inborn genetic diseases.

What condition is associated with DSPP p.Asp1071Val (c.3212A>T)?

DSPP p.Asp1071Val (c.3212A>T) is associated with Inborn genetic diseases (ClinVar).

How common is DSPP p.Asp1071Val (c.3212A>T) in the general population?

DSPP p.Asp1071Val (c.3212A>T) is very rare (popmax 8.75e-05%, nfe) (gnomAD).

What do computational predictors say about DSPP p.Asp1071Val (c.3212A>T)?

AlphaMissense predicts likely benign (score 0.3098) — an in-silico prediction, not a clinical call.

DSPP p.Asp1071Val

c.3212A>T · VCV3842731

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.3098 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 8.75e-05%, nfe)

Missense predictors

1/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.3098	likely benign
REVEL	0.244	benign-leaning
SaProt	LLR -13.59	damaging
⇒ SaProt calls this damaging; AlphaMissense and REVEL do not.
Splicing
SpliceAI	—	not looked up on this page · why
Constraint at this position
Conservation	phyloP 1.8	GERP -0.25, phastCons 0.008
Regional constraint	o/e 0.38	unconstrained · MANE · 513 bp · p 9.7e-18 · regional, not allelic
Overall
CADD	18.51	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

Grpmax group 8.75e-05% European (non-Finnish) · 1/1,142,514 alleles

Overall 7.19e-05% 1/1,391,020 alleles · very rare

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: DSPP
Protein: p.Asp1071Val
Coding: c.3212A>T
Type: single nucleotide variant
Location: chr4:87615874 (GRCh38)

Full DSPP 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

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/dspp-p-asp1071val (accessed [today's date]).

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