CDT1 p.Val6fs
c.16del · rs2508191996 · VCV1972396
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Consequence | frameshift | predicted loss-of-function |
|---|---|---|
| NMD | predicted | premature termination codon in exon 1 of 10 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP -1.3 | GERP -2 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Population frequency
No gnomAD frequency available for this variant. This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.
Variant & gene context
- Gene
- CDT1
- Protein
- p.Val6fs
- Coding
- c.16del
- MANE Select
- NM_030928
- dbSNP
- rs2508191996
- Type
- Deletion
- Location
- chr16:88803847 (GRCh38)
- Gene constraint
- LOEUF 1.737 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 74.51 · 6 PDB
- Residue 6
- the 'disordered' region; a turn
Similar variants
- CDT1 c.488+16del Benign/Likely benign ★★ same type
- CDT1 p.Ala360del Pathogenic ★ same type
- CDT1 p.Gln446fs Pathogenic ★ same type
- CDT1 p.Leu25fs Pathogenic ★ same type
- CDT1 p.Phe465fs Pathogenic ★ same type
- CDT1 c.228+27_228+55del Likely benign ★ same type
- CDT1 c.351+8del Benign ★ same type
- CDT1 c.352-14del Likely 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/cdt1-p-val6fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown