CDSN p.Ser395Gly
c.1183A>G · VCV3831057
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 8.56e-05%, nfe)
Conditions
1
Inborn genetic diseases
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| REVEL | 0.027 | moderately benign-leaning |
|---|---|---|
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP -3.1 | |
| Overall | ||
| CADD | 0.031 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
8.56e-05%
European (non-Finnish) · 1/1,168,412 alleles
Overall
6.95e-05%
1/1,438,650 alleles · very rare
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
- CDSN
- Protein
- p.Ser395Gly
- Coding
- c.1183A>G
- MANE Select
- NM_001264
- Type
- single nucleotide variant
- Location
- chr6:31116432 (GRCh38)
- Gene constraint
- LOEUF 0.77 · pLI 0.08 (gnomAD)
- Structure
- AlphaFold pLDDT 38.13
- Residue 395
- the 'disordered' region
Similar variants
- CDSN p.Cys423Ser Uncertain significance ★★ same condition
- CDSN p.Gly335Ala Uncertain significance ★★ same condition
- CDSN p.Pro226Ser Uncertain significance ★★ same condition
- CDSN p.Pro471Leu Uncertain significance ★★ same condition
- CDSN p.Ser159Gly Uncertain significance ★★ same condition
- CDSN p.Ser274Asn Uncertain significance ★★ same condition
- CDSN p.Val506Met Uncertain significance ★★ same condition
- CDSN p.Pro192Leu Likely benign ★★ 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/cdsn-p-ser395gly (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown