ROBO3 p.Arg334=
c.1002C>T · rs748933110 · VCV736457
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.0718%, sas)
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 -14 | GERP -3 |
| Overall | ||
| CADD | 0.125 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.0718%
South Asian · 65/90,524 alleles
Filtering AF
0.0578%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.0527%
Overall
0.00738%
119/1,612,244 alleles · ultra-rare
exomes 108/1,460,098 · genomes 11/152,146 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| South Asiangrpmax | 0.0718% | 1,393 |
| Middle Eastern | 0.0329% | 3,042 |
| Ashkenazi Jewishnot grpmax-eligible | 0.0203% | 4,925 |
| European (non-Finnish) | 0.00356% | 28,079 |
| Remaining individualsnot grpmax-eligible | 0.0032% | 31,216 |
| Admixed American | 0.00167% | 59,750 |
| African / African-American | 0.00134% | 74,878 |
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
- ROBO3
- Protein
- p.Arg334=
- Coding
- c.1002C>T
- MANE Select
- NM_022370
- dbSNP
- rs748933110
- Type
- single nucleotide variant
- Location
- chr11:124870697 (GRCh38)
- Gene constraint
- LOEUF 0.749 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 63.99 · 3 PDB
- Residue 334
- the ig-like c2-type 3 domain
Similar variants
- ROBO3 c.767-1G>A Pathogenic/Likely pathogenic ★★ same type
- ROBO3 p.Arg245Trp Likely pathogenic ★★ same type
- ROBO3 p.Arg703Pro Likely pathogenic ★★ same type
- ROBO3 p.Ile95Thr Likely pathogenic ★★ same type
- ROBO3 p.Pro771Leu Likely pathogenic ★★ ⚠ same type
- ROBO3 c.*67C>T Uncertain significance ★★ same type
- ROBO3 p.Ala669= Uncertain significance ★★ same type
- ROBO3 p.Ala900Val 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/robo3-p-arg334 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown