Is FLRT1 p.Asn95= (c.285C>T) pathogenic?

FLRT1 p.Asn95= (c.285C>T) is classified Likely benign in FLRT1 (ClinVar, Single submitter, 1 submitter; last evaluated 2020-10-28). Very rare (popmax 0.00666%, afr); Associated with peripheral neuropathy.

What condition is associated with FLRT1 p.Asn95= (c.285C>T)?

FLRT1 p.Asn95= (c.285C>T) is associated with peripheral neuropathy (ClinVar).

How common is FLRT1 p.Asn95= (c.285C>T) in the general population?

FLRT1 p.Asn95= (c.285C>T) is very rare (popmax 0.00666%, afr) (gnomAD).

FLRT1 p.Asn95=

c.285C>T · rs201354922 · VCV1128795

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00666%, afr)

Conditions

peripheral neuropathy

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 -9.8	GERP -4
Overall
CADD	0.094	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00666% African / African-American · 5/75,044 alleles

Filtering AF 0.00286% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00236%

Overall 0.00347% 56/1,614,076 alleles · very rare exomes 48/1,461,774 · genomes 8/152,302 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.00666%	15,009
South Asian	0.00659%	15,180
European (non-Finnish)	0.00356%	28,095
East Asian	0.00223%	44,872
Remaining individualsnot grpmax-eligible	0.0016%	62,498
Finnishnot grpmax-eligible	0.00156%	64,008

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: FLRT1
Protein: p.Asn95=
Coding: c.285C>T
MANE Select: NM_013280
dbSNP: rs201354922
Type: single nucleotide variant
Location: chr11:64116552 (GRCh38)
Gene constraint: LOEUF 0.682 · pLI 0.14 (gnomAD)
Structure: AlphaFold pLDDT 73.46

Full FLRT1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

Similar variants

FLRT1 p.Ala148Gly Uncertain significance ★★ same condition
FLRT1 p.Ala461Thr Uncertain significance ★★ same condition
FLRT1 p.Arg149Cys Uncertain significance ★★ same condition
FLRT1 p.Arg326Lys Uncertain significance ★★ same condition
FLRT1 p.Arg452His Uncertain significance ★★ same condition
FLRT1 p.Arg586Gln Uncertain significance ★★ same condition
FLRT1 p.Arg592Gln Uncertain significance ★★ same condition
FLRT1 p.Arg592Trp Uncertain significance ★★ 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/flrt1-p-asn95 (accessed [today's date]).

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