ROGDI p.Phe217=
c.651C>T · rs773539275 · VCV1122616
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.0134%, amr)
Conditions
1
amelocerebrohypohidrotic syndrome
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 9.9 | GERP 1.7, phastCons 1 |
| Overall | ||
| CADD | 8.086 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.0134%
Admixed American · 8/59,810 alleles
Filtering AF
0.00663%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00484%
Overall
0.000497%
8/1,608,446 alleles · ultra-rare
exomes 6/1,456,288 · genomes 2/152,158 · joint denominator
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
- ROGDI
- Protein
- p.Phe217=
- Coding
- c.651C>T
- MANE Select
- NM_024589
- dbSNP
- rs773539275
- Type
- single nucleotide variant
- Location
- chr16:4797982 (GRCh38)
- Gene constraint
- LOEUF 1.648 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 89.59 · 2 PDB
- Residue 217
- a UniProt-annotated variant site (in ktzs; uncertain significance); a UniProt-annotated variant site (in ktzs)
Similar variants
- ROGDI c.117+1G>A Pathogenic/Likely pathogenic ★★ same condition
- ROGDI c.46-2A>G Likely pathogenic ★★ same condition
- ROGDI c.531+5G>C Likely pathogenic ★★ same condition
- ROGDI c.645+2T>A Likely pathogenic ★★ same condition
- ROGDI p.Arg157Ter Pathogenic ★★ same condition
- ROGDI p.Gln112Ter Pathogenic/Likely pathogenic ★★ same condition
- ROGDI p.Gln114Ter Pathogenic/Likely pathogenic ★★ same condition
- ROGDI p.Gln96Ter Pathogenic ★★ same condition
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/rogdi-p-phe217 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown