C12S (p.Cys12Ser) variant of KIT (P10721)
C12S (p.Cys12Ser) in KIT (P10721) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Gastrointestinal stromal tumor. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes published literature and structural context.
C12S (p.Cys12Ser) variant details
- p.Cys12Ser
- rs1716941861
- ClinGen CA356897943
- ClinVar RCV001044765
- Ensembl rs1716941861
- Uncertain significance
- Gastrointestinal stromal tumor
- Missense
- Variant Prioritization Score for Impact Estimate 0.325
- AlphaMissense 0.08
- MetaLR 0.14
- MetaSVM -0.92
- PolyPhen-2 0.00
- SIFT 0.78
- MutPred 0.58
- ClinVar: Uncertain significance (Gastrointestinal stromal tumor)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: The UK NEQAS for Molecular Genetics scheme for gastrointestinal stromal tumour: findings and recommendations following… (PMID 22685257)
- Cited in: Tumor markers in colorectal cancer, gastric cancer and gastrointestinal stromal cancers: European group on tumor… (PMID 23852704)