TRIM37 p.Arg166=
c.498G>A · rs2043120433 · VCV1987117
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00267%, 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 3.4 | GERP 1.4, phastCons 1 |
| Overall | ||
| CADD | 9.451 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00267%
African / African-American · 2/75,032 alleles
Filtering AF
0.000442%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.000166%
Overall
0.000124%
2/1,613,828 alleles · very rare
exomes 2/1,461,552 · genomes 0/152,276 · 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
- TRIM37
- Protein
- p.Arg166=
- Coding
- c.498G>A
- MANE Select
- NM_015294
- dbSNP
- rs2043120433
- Type
- single nucleotide variant
- Location
- chr17:59079872 (GRCh38)
- Gene constraint
- LOEUF 0.789 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 64.93 · 1 PDB
Similar variants
- TRIM37 c.1020-1G>C Likely pathogenic ★★ same type
- TRIM37 c.1948+2T>C Likely pathogenic ★★ same type
- TRIM37 c.1949-12A>G Likely pathogenic ★★ same type
- TRIM37 c.370-1G>A Pathogenic/Likely pathogenic ★★ same type
- TRIM37 c.493-2A>G Pathogenic ★★ same type
- TRIM37 c.617-1G>A Likely pathogenic ★★ same type
- TRIM37 p.Arg14Ter Likely pathogenic ★★ same type
- TRIM37 p.Arg361Ter Pathogenic/Likely pathogenic ★★ 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/trim37-p-arg166 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown