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BTRC p.Tyr130Cys

c.389A>G · VCV3993655

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
ambiguous
0.4969 · ACMG-weighted
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
AlphaMissense0.4969ambiguous
REVEL0.344indeterminate
SaProtLLR -8.99tolerated
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP 11GERP 2.6, phastCons 1
Regional constrainto/e 0.90unconstrained · MANE · 168 kb · p 0.19 · regional, not allelic
Overall
CADD28.1PHRED · 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
BTRC
Protein
p.Tyr130Cys
Coding
c.389A>G
MANE Select
NM_033637
Type
single nucleotide variant
Location
chr10:101521703 (GRCh38)
Gene constraint
LOEUF 0.643 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 80.33 · 15 PDB
Residue 130
an α-helix; the 'homodimerization domain d' region
Full BTRC 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/btrc-p-tyr130cys (accessed [today's date]).

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