DPYD p.Thr93=
c.279T>C · rs2101070143 · VCV1694519
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
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 -0.85 | GERP -3.1 |
| Overall | ||
| CADD | 1.925 | PHRED · no single calibrated threshold — expert panels disagree |
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
- DPYD
- Protein
- p.Thr93=
- Coding
- c.279T>C
- MANE Select
- NM_000110
- dbSNP
- rs2101070143
- Type
- single nucleotide variant
- Location
- chr1:97740434 (GRCh38)
- Gene constraint
- LOEUF 1.09 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 96.23
- Residue 93
- the 4fe-4s ferredoxin-type 1 domain
Similar variants
- DPYD c.1340-2A>C Likely pathogenic ★★ same type
- DPYD c.1905+1G>C Pathogenic/Likely pathogenic ★★ same type
- DPYD c.233+1G>T Likely pathogenic ★★ same type
- DPYD c.2622+1G>A Likely pathogenic ★★ same type
- DPYD c.2767-1G>A Likely pathogenic ★★ same type
- DPYD c.680+1G>T Likely pathogenic ★★ same type
- DPYD p.Arg21Ter Pathogenic/Likely pathogenic ★★ same type
- DPYD p.Arg561Ter 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/dpyd-p-thr93 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown