DACT1 p.Val341=
c.1023C>T · rs863091 · VCV3059824
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 2 submitters
gnomAD v4.1
Common
common (popmax 38.5%, afr) — too common for a highly-penetrant pathogenic allele
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 1.7 | GERP -0.18, phastCons 0.94 |
| Overall | ||
| CADD | 9.741 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
38.5%
African / African-American · 28,890/75,002 alleles
Filtering AF
38.1%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 38%
Overall
20.2%
325,581/1,614,080 alleles · common
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 38.5% | 3 |
| Admixed American | 34% | 3 |
| Middle Eastern | 27.9% | 4 |
| Ashkenazi Jewishnot grpmax-eligible | 24.3% | 4 |
| Remaining individualsnot grpmax-eligible | 21.3% | 5 |
| South Asian | 20.8% | 5 |
| European (non-Finnish) | 18.4% | 5 |
| Finnishnot grpmax-eligible | 17.9% | 6 |
| East Asian | 13.4% | 7 |
| Amishnot grpmax-eligible | 12.6% | 8 |
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
- DACT1
- Protein
- p.Val341=
- Coding
- c.1023C>T
- MANE Select
- NM_001079520
- dbSNP
- rs863091
- Type
- single nucleotide variant
- Location
- chr14:58645757 (GRCh38)
- Gene constraint
- LOEUF 0.703 · pLI 0.17 (gnomAD)
- Structure
- AlphaFold pLDDT 50.95
Similar variants
- DACT1 p.Glu451Asp Uncertain significance ★★ ⚠ same type
- DACT1 c.635-121T>C Likely benign ★★ same type
- DACT1 p.Ala427Val Benign ★★ same type
- DACT1 p.Ala500= Benign ★★ same type
- DACT1 p.Asp409Asn Benign ★★ same type
- DACT1 p.Glu257Lys Benign/Likely benign ★★ same type
- DACT1 p.Glu49= Likely benign ★★ same type
- DACT1 p.Gly660Ser 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/dact1-p-val341 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown