CD151 p.Gly193=
c.579G>A · rs1130663 · VCV1277016
Benign
Multiple submitters
Classification
Benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 5 submitters
gnomAD v4.1
Common
common (popmax 88.6%, eas) — too common for a highly-penetrant pathogenic allele
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 -0.061 | GERP -4 |
| Overall | ||
| CADD | 3.721 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
88.6%
East Asian · 39,725/44,838 alleles
Filtering AF
87.9%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 87.6%
Overall
68.1%
1,098,462/1,612,376 alleles · common
| Ancestry group | Frequency | 1 in |
|---|---|---|
| East Asiangrpmax | 88.6% | 1 |
| Admixed American | 78.9% | 1 |
| Finnishnot grpmax-eligible | 75.2% | 1 |
| Amishnot grpmax-eligible | 73.6% | 1 |
| European (non-Finnish) | 69.6% | 1 |
| Remaining individualsnot grpmax-eligible | 65.4% | 2 |
| African / African-American | 53.3% | 2 |
| Middle Eastern | 51.3% | 2 |
| Ashkenazi Jewishnot grpmax-eligible | 48.9% | 2 |
| South Asian | 48.4% | 2 |
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
- CD151
- Protein
- p.Gly193=
- Coding
- c.579G>A
- MANE Select
- NM_004357
- dbSNP
- rs1130663
- Type
- single nucleotide variant
- Location
- chr11:837582 (GRCh38)
- Gene constraint
- LOEUF 0.816 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 88.02
Similar variants
- CD151 p.Lys7Ter Pathogenic ★★ same type
- CD151 c.352-11C>G Uncertain significance ★★ same type
- CD151 c.702+4A>G Uncertain significance ★★ same type
- CD151 c.702+5G>C Uncertain significance ★★ same type
- CD151 p.Ala145Thr Uncertain significance ★★ ⚠ same type
- CD151 p.Ala81Thr Uncertain significance ★★ ⚠ same type
- CD151 p.Arg133Cys Uncertain significance ★★ same type
- CD151 p.Arg165Gln 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/cd151-p-gly193 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown