Is APOLTP p.Lys2349= (c.7047G>A) pathogenic?

APOLTP p.Lys2349= (c.7047G>A) is classified Likely benign in APOLTP (ClinVar, Single submitter, 1 submitter; last evaluated 2022-05-01). Very rare (popmax 0.000442%, nfe).

How common is APOLTP p.Lys2349= (c.7047G>A) in the general population?

APOLTP p.Lys2349= (c.7047G>A) is very rare (popmax 0.000442%, nfe) (gnomAD).

APOLTP p.Lys2349=

c.7047G>A · rs1232165169 · VCV2646218

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.000442%, nfe)

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 -0.38	GERP -0.051
Overall
CADD	0.589	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.000442% European (non-Finnish) · 1/226,106 alleles

Overall 0.000405% 1/246,778 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: APOLTP
Protein: p.Lys2349=
Coding: c.7047G>A
MANE Select: NM_001370704
dbSNP: rs1232165169
Type: single nucleotide variant
Location: chr16:11407245 (GRCh38)
Structure: AlphaFold pLDDT 87.88

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

Similar variants

APOLTP p.Arg1455Gln Likely benign ★ same type
APOLTP p.Arg179= Likely benign ★ same type
APOLTP p.Asn1704= Likely benign ★ same type
APOLTP p.Glu2187= Likely benign ★ same type
APOLTP p.His1059= Likely benign ★ same type
APOLTP p.His897= Likely benign ★ same type
APOLTP p.Pro1959= Likely benign ★ same type
APOLTP p.Ser1894= Likely benign ★ same type

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/apoltp-p-lys2349 (accessed [today's date]).

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