S7G (p.Ser7Gly) variant of CDH1 (Cadherin-1)
S7G (p.Ser7Gly) in CDH1 (Cadherin-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary diffuse gastric adenocarcinoma. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
S7G (p.Ser7Gly) variant details
- p.Ser7Gly
- rs1303550652
- ClinGen CA396451299
- ClinVar RCV003229660
- gnomAD rs1303550652
- Uncertain significance
- Hereditary diffuse gastric adenocarcinoma
- Missense
- Variant Prioritization Score for Impact Estimate 0.314
- AlphaMissense 0.06
- MetaLR 0.07
- MetaSVM -1.01
- PolyPhen-2 0.00
- SIFT 0.65
- MutPred 0.40
- ClinVar: Uncertain significance (Hereditary diffuse gastric adenocarcinoma)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- Cited in: American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. (PMID 17392385)
- Cited in: American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility. (PMID 20065170)