RAB39B p.Pro195=
c.585A>T · rs1602912605 · VCV761788
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
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 -0.68, phastCons 0.28 |
| Overall | ||
| CADD | 7.152 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- RAB39B
- Protein
- p.Pro195=
- Coding
- c.585A>T
- MANE Select
- NM_171998
- dbSNP
- rs1602912605
- Type
- single nucleotide variant
- Location
- chrX:155260860 (GRCh38)
- Structure
- AlphaFold pLDDT 88.67 · 1 PDB
- Residue 195
- a UniProt-annotated variant site (in wsmn)
Similar variants
- RAB39B p.Gly178Arg Uncertain significance ★★ ⚠ same type
- RAB39B p.Ser96Phe Uncertain significance ★★ ⚠ same type
- RAB39B p.Thr129Ile Uncertain significance ★★ ⚠ same type
- RAB39B c.*1347C>T Benign ★★ same type
- RAB39B c.*1656= Benign ★★ same type
- RAB39B p.Gly31= Benign/Likely benign ★★ same type
- RAB39B p.Gly42= Benign/Likely benign ★★ same type
- RAB39B p.His110= Benign/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/rab39b-p-pro195 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown