Is BLM p.Asp997= (c.2991T>C) pathogenic?

BLM p.Asp997= (c.2991T>C) is classified Likely benign in BLM (ClinVar, Single submitter, 1 submitter; last evaluated 2025-01-06). Absent from gnomAD v4.1; Associated with Bloom syndrome.

What condition is associated with BLM p.Asp997= (c.2991T>C)?

BLM p.Asp997= (c.2991T>C) is associated with Bloom syndrome (ClinVar).

How common is BLM p.Asp997= (c.2991T>C) in the general population?

BLM p.Asp997= (c.2991T>C) is absent from gnomAD v4.1 (gnomAD).

How is Bloom syndrome inherited?

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

BLM p.Asp997=

c.2991T>C · VCV3700875

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

Bloom syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · T>G here scores Δ0.91 · evaluated, not missing
Constraint at this position
Conservation	phyloP -4	GERP -5
Overall
CADD	3.861	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: BLM
Protein: p.Asp997=
Coding: c.2991T>C
MANE Select: NM_000057
Type: single nucleotide variant
Location: chr15:90790816 (GRCh38)
Gene constraint: LOEUF 0.847 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 61.10 · 16 PDB
Residue 997: an α-helix; the helicase c-terminal domain

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

Disease context

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

For Bloom syndrome (Orphanet):

Inheritance: Autosomal recessive
Onset: Antenatal, Neonatal
Prevalence: 1-9 / 100 000 (Specific population)

Similar variants

BLM p.Asp997Asn Uncertain significance ★★ ⚠ same residue
BLM p.Asp997Val Uncertain significance ★ ⚠ same residue
BLM p.Asp997Gly Uncertain significance ★ ⚠ same residue
BLM p.Asp997Glu Uncertain significance ⚠ same residue
BLM c.1087+1G>A Likely pathogenic ★★ same condition
BLM c.1088-1G>A Likely pathogenic ★★ same condition
BLM c.1220+2T>C Likely pathogenic ★★ same condition
BLM c.1220+2T>G 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/blm-p-asp997 (accessed [today's date]).

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