DHH p.Ala368=
c.1104G>C · rs1338004115 · VCV3042896
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 2 submitters
gnomAD v4.1
Rare
very rare (popmax 0.00404%, 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 0.33 | GERP -0.34, phastCons 0.98 |
| Overall | ||
| CADD | 10.33 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00404%
African / African-American · 3/74,266 alleles
Filtering AF
0.00107%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.000497%
Overall
0.00019%
3/1,579,170 alleles · very rare
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
- DHH
- Protein
- p.Ala368=
- Coding
- c.1104G>C
- MANE Select
- NM_021044
- dbSNP
- rs1338004115
- Type
- single nucleotide variant
- Location
- chr12:49089946 (GRCh38)
- Gene constraint
- LOEUF 0.999 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 84.87 · 5 PDB
- Residue 368
- a UniProt-annotated variant site (in gdmn; uncertain significance); a UniProt-annotated variant site (in gdmn)
Similar variants
- DHH c.*401G>T Uncertain significance ★★ same type
- DHH p.Ala287Glu Uncertain significance ★★ ⚠ same type
- DHH p.Arg102His Uncertain significance ★★ ⚠ same type
- DHH p.Arg309Leu Uncertain significance ★★ ⚠ same type
- DHH p.Arg318Pro Uncertain significance ★★ ⚠ same type
- DHH p.Ser210Arg Uncertain significance ★★ ⚠ same type
- DHH c.303+66C>T Benign ★★ same type
- DHH c.304-15T>C 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/dhh-p-ala368 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown