V20F (p.Val20Phe) variant of KIT (P10721)
V20F (p.Val20Phe) 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; Hereditary cancer-predisposing syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes published literature and structural context.
V20F (p.Val20Phe) variant details
- p.Val20Phe
- rs1553881787
- ClinGen CA356898011
- ClinVar RCV000633811
- ClinVar RCV004025432
- Uncertain significance
- Gastrointestinal stromal tumor; Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.333
- AlphaMissense 0.08
- MetaLR 0.20
- MetaSVM -0.96
- PolyPhen-2 0.01
- SIFT 0.10
- MutPred 0.48
- ClinVar: Uncertain significance (Gastrointestinal stromal tumor; Hereditary cancer-predisposing s)
- 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)