DGAT2 p.Phe136=
c.408T>C · rs150822096 · VCV782870
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.399%, eas)
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 -0.24 | GERP -0.92, phastCons 0.51 |
| Overall | ||
| CADD | 5.584 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.399%
East Asian · 179/44,884 alleles
Filtering AF
0.351%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.333%
Overall
0.0129%
208/1,614,198 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| East Asiangrpmax | 0.399% | 251 |
| Remaining individualsnot grpmax-eligible | 0.0448% | 2,232 |
| European (non-Finnish) | 8.47e-05% | 1,180,040 |
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
- DGAT2
- Protein
- p.Phe136=
- Coding
- c.408T>C
- MANE Select
- NM_032564
- dbSNP
- rs150822096
- Type
- single nucleotide variant
- Location
- chr11:75790710 (GRCh38)
- Gene constraint
- LOEUF 0.93 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 88.52
Similar variants
- DGAT2 p.Glu15Val Uncertain significance ★★ ⚠ same type
- DGAT2 p.Ile313Val Uncertain significance ★★ ⚠ same type
- DGAT2 p.Tyr223Ser Uncertain significance ★★ ⚠ same type
- DGAT2 p.Arg297Gln Benign/Likely benign ★★ ⚠ same type
- DGAT2 p.Gly318Ser Likely benign ★★ ⚠ same type
- DGAT2 p.Ile355= Likely benign ★★ same type
- DGAT2 p.Ser230= Benign/Likely benign ★★ same type
- DGAT2 p.Ala253Val Uncertain significance ★ ⚠ 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/dgat2-p-phe136 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown