Is INF2 p.Ser186= (c.558C>T) pathogenic?

INF2 p.Ser186= (c.558C>T) is classified Benign/Likely benign in INF2 (ClinVar, Multiple submitters, 9 submitters; last evaluated 2026-01-02). Rare (popmax 0.433%, afr); Associated with Inborn genetic diseases.

What condition is associated with INF2 p.Ser186= (c.558C>T)?

INF2 p.Ser186= (c.558C>T) is associated with Inborn genetic diseases, focal segmental glomerulosclerosis 5, Charcot-Marie-Tooth disease dominant intermediate E (ClinVar).

How common is INF2 p.Ser186= (c.558C>T) in the general population?

INF2 p.Ser186= (c.558C>T) is rare (popmax 0.433%, afr) (gnomAD).

INF2 p.Ser186=

c.558C>T · rs150714865 · VCV540059

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 9 submitters

gnomAD v4.1

Rare

rare (popmax 0.433%, afr)

Conditions

Inborn genetic diseases

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation/SpliceAI carries the signal.
Splicing
SpliceAI	Δ0.20	acceptor gain · deltas
Constraint at this position
Conservation	phyloP -20	GERP -14
Overall
CADD	0.699	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.433% African / African-American · 325/75,064 alleles

Filtering AF 0.394% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.379%

Overall 0.0371% 599/1,613,126 alleles · rare exomes 376/1,460,764 · genomes 223/152,362 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.433%	231
East Asian	0.0535%	1,870
Remaining individualsnot grpmax-eligible	0.04%	2,500
Admixed American	0.0366%	2,729
Middle Eastern	0.033%	3,031
European (non-Finnish)	0.017%	5,900
South Asian	0.0011%	91,090

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: INF2
Protein: p.Ser186=
Coding: c.558C>T
MANE Select: NM_022489
dbSNP: rs150714865
Type: single nucleotide variant
Location: chr14:104703345 (GRCh38)
Gene constraint: LOEUF 0.526 · pLI 0.33 · ClinGen HI 0/3 (gnomAD)
Structure: AlphaFold pLDDT 67.34 · 10 PDB
Residue 186: the gbd/fh3 domain; a UniProt-annotated variant site (in fsgs5)

Full INF2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: focal segmental glomerulosclerosis 5 Charcot-Marie-Tooth disease dominant intermediate E

Similar variants

INF2 p.Ser186Pro Likely pathogenic ★ same residue
INF2 p.Arg177Cys Pathogenic/Likely pathogenic ★★ same condition
INF2 p.Arg214Cys Pathogenic/Likely pathogenic ★★ same condition
INF2 p.Arg214His Pathogenic/Likely pathogenic ★★ same condition
INF2 p.Arg218Gln Pathogenic/Likely pathogenic ★★ same condition
INF2 p.Arg218Trp Pathogenic/Likely pathogenic ★★ same condition
INF2 p.Arg91Gly Pathogenic/Likely pathogenic ★★ same condition
INF2 p.Asn202Asp 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/inf2-p-ser186 (accessed [today's date]).

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