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TACO1 p.Pro118=

c.354C>T · rs1258783051 · VCV3034268

Likely benign No assertion criteria
Classification
Likely benign
ClinVar
Review
No assertion criteria ☆☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00167%, amr)
Conditions
1
TACO1-related disorder

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
ConservationphyloP 1.3GERP 0.51, phastCons 1
Overall
CADD12.84PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes
Grpmax group 0.00167% Admixed American · 1/60,008 alleles
Overall 6.2e-05% 1/1,614,088 alleles · very rare exomes 1/1,461,862 · genomes 0/152,226 · joint denominator

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
TACO1
Protein
p.Pro118=
Coding
c.354C>T
MANE Select
NM_016360
dbSNP
rs1258783051
Type
single nucleotide variant
Location
chr17:63604607 (GRCh38)
Gene constraint
LOEUF 0.848 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 84.91 · 8 PDB
Full TACO1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

TACO1-related disorder

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/taco1-p-pro118 (accessed [today's date]).

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