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FLRT1 p.Leu355His

c.1064T>A · VCV4025669

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
REVEL0.258benign-leaning
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP 5GERP 2, phastCons 1
Regional constrainto/e 0.78unconstrained · MANE · 2,021 bp · p 5.7e-12 · regional, not allelic
Overall
CADD25.0PHRED · 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
FLRT1
Protein
p.Leu355His
Coding
c.1064T>A
MANE Select
NM_013280
Type
single nucleotide variant
Location
chr11:64117331 (GRCh38)
Gene constraint
LOEUF 0.682 · pLI 0.14 (gnomAD)
Structure
AlphaFold pLDDT 73.46
Residue 355
the lrrct domain
Full FLRT1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/flrt1-p-leu355his (accessed [today's date]).

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