G307S (p.Gly307Ser) variant of COL4A5 (Collagen alpha-5(IV) chain)
G307S (p.Gly307Ser) in COL4A5 (Collagen alpha-5(IV) chain) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic/likely pathogenic in the context of not provided; X-linked Alport syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.88 / 1. The record also includes population frequency data, published literature, and structural context.
G307S (p.Gly307Ser) variant details
- p.Gly307Ser
- rs2147777425
- ClinGen CA413926949
- cosmic curated COSV10645
- ClinVar RCV002028076
- Pathogenic/Likely pathogenic
- not provided; X-linked Alport syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.88
- REVEL 0.98
- AlphaMissense 0.46
- MetaLR 0.99
- MetaSVM 0.99
- CADD 28.50
- PolyPhen-2 1.00
- ClinVar: Pathogenic/Likely pathogenic (not provided; X-linked Alport syndrome)
- EBI: Pathogenic
- UniProt: Pathogenic
- Most common in the Non-Finnish European population (allele frequency 2.5e-05)
- Structural context available
- Cited in: Alport Syndrome. (PMID 20301386)
- Cited in: Clinical utility gene card for: Alport syndrome. (PMID 22166944)