Is MTTP p.Met877Val (c.2629A>G) pathogenic?

MTTP p.Met877Val (c.2629A>G) is classified Uncertain significance in MTTP (ClinVar, Single submitter, 2 submitters; last evaluated 2024-02-19). AlphaMissense: ambiguous (0.36); Absent from gnomAD v4.1; Associated with abetalipoproteinemia.

What condition is associated with MTTP p.Met877Val (c.2629A>G)?

MTTP p.Met877Val (c.2629A>G) is associated with abetalipoproteinemia (ClinVar).

How common is MTTP p.Met877Val (c.2629A>G) in the general population?

MTTP p.Met877Val (c.2629A>G) is absent from gnomAD v4.1 (gnomAD).

How is Abetalipoproteinemia inherited?

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

What do computational predictors say about MTTP p.Met877Val (c.2629A>G)?

AlphaMissense predicts ambiguous (score 0.36) — an in-silico prediction, not a clinical call.

MTTP p.Met877Val

c.2629A>G · rs1726272076 · VCV970450

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

AlphaMissense

ambiguous

0.36 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

abetalipoproteinemia

Computational evidence

Protein change
AlphaMissense	0.36	ambiguous
REVEL	0.557	indeterminate
SaProt	LLR -6.65	tolerated
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Pangolin	Δ0.28	gain · loss 0.00 · not in the SpliceAI release · independent
Constraint at this position
Conservation	phyloP 11	GERP 1.9, phastCons 1
Regional constraint	o/e 0.89	unconstrained · MANE · 48 kb · p 0.00018 · regional, not allelic
Overall
CADD	22.3	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

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: MTTP
Protein: p.Met877Val
Coding: c.2629A>G
MANE Select: NM_001386140
dbSNP: rs1726272076
Type: single nucleotide variant
Location: chr4:99622792 (GRCh38)
Gene constraint: LOEUF 0.672 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 86.73 · 2 PDB
Residue 877: an α-helix

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

Disease context

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

For Abetalipoproteinemia (Orphanet):

Inheritance: Autosomal recessive
Onset: Childhood, Infancy
Prevalence: <1 / 1 000 000 (Worldwide)

Similar variants

MTTP c.1067+1G>C Likely pathogenic ★★ same condition
MTTP c.1769+2T>C Pathogenic/Likely pathogenic ★★ same condition
MTTP c.1867+1G>A Pathogenic ★★ same condition
MTTP c.1867+5G>A Pathogenic/Likely pathogenic ★★ same condition
MTTP c.1868-2A>G Likely pathogenic ★★ same condition
MTTP c.2342+1G>A Pathogenic ★★ same condition
MTTP c.502-1G>C Likely pathogenic ★★ same condition
MTTP c.502-2A>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/mttp-p-met877val (accessed [today's date]).

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