BTRC p.Ile168=
c.504A>T · rs760375120 · VCV1534940
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00534%, afr)
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 6.6 | GERP -2.3, phastCons 1 |
| Overall | ||
| CADD | 11.78 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00534%
African / African-American · 4/74,926 alleles
Filtering AF
0.00175%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00104%
Overall
0.00031%
5/1,613,956 alleles · very rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 0.00534% | 18,732 |
| European (non-Finnish) | 8.47e-05% | 1,179,966 |
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
- BTRC
- Protein
- p.Ile168=
- Coding
- c.504A>T
- MANE Select
- NM_033637
- dbSNP
- rs760375120
- Type
- single nucleotide variant
- Location
- chr10:101521818 (GRCh38)
- Gene constraint
- LOEUF 0.643 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 80.33 · 15 PDB
- Residue 168
- an α-helix; the 'homodimerization domain d' region
Similar variants
- BTRC p.Leu271Phe Uncertain significance ★★ ⚠ same type
- BTRC p.Leu86Phe Uncertain significance ★★ ⚠ same type
- BTRC c.556+7C>G Benign ★★ same type
- BTRC p.Ala543Ser Benign ★★ same type
- BTRC p.Ile229= Benign ★★ same type
- BTRC p.Leu387= Likely benign ★★ same type
- BTRC p.Pro592Arg Likely benign ★★ same type
- BTRC p.Pro592His Benign ★★ ⚠ same type
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-ile168 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown