TRMU p.Asp413=
c.1239T>C · rs758409354 · VCV1154488
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.0011%, sas)
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 -8.4 | GERP -2.1 |
| Overall | ||
| CADD | 0.087 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.0011%
South Asian · 1/91,092 alleles
Overall
0.000124%
2/1,613,434 alleles · very rare
exomes 1/1,461,240 · genomes 1/152,194 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| South Asiangrpmax | 0.0011% | 91,092 |
| European (non-Finnish) | 8.47e-05% | 1,180,006 |
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
- TRMU
- Protein
- p.Asp413=
- Coding
- c.1239T>C
- MANE Select
- NM_018006
- dbSNP
- rs758409354
- Type
- single nucleotide variant
- Location
- chr22:46356979 (GRCh38)
- Gene constraint
- LOEUF 1.276 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 89.60
- Residue 413
- the 'disordered' region
Similar variants
- TRMU c.1019-1G>A Likely pathogenic ★★ same type
- TRMU c.1102-3C>G Likely pathogenic ★★ same type
- TRMU c.248+1G>A Pathogenic/Likely pathogenic ★★ same type
- TRMU c.249-2A>G Likely pathogenic ★★ same type
- TRMU c.355+1G>C Likely pathogenic ★★ same type
- TRMU c.355+1G>T Likely pathogenic ★★ same type
- TRMU c.478+1G>A Likely pathogenic ★★ same type
- TRMU c.652-2A>G 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/trmu-p-asp413 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown