M237V (p.Met237Val) variant of TP53 (Cellular tumor antigen p53)
M237V (p.Met237Val) in TP53 (Cellular tumor antigen p53) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as conflicting interpretations in the context of Hereditary cancer-predisposing syndrome; not specified; Li-Fraumeni syndrome 1. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data, published literature, and structural context.
M237V (p.Met237Val) variant details
- p.Met237Val
- rs730882004
- ClinGen CA000348
- NCI-TCGA Cosmic COSV5270
- cosmic curated COSV52701
- Conflicting interpretations
- Hereditary cancer-predisposing syndrome; not specified; Li-Fraumeni syndrome 1
- Missense
- Variant Prioritization Score for Impact Estimate 0.796
- REVEL 0.94
- ESM-1b 1.00
- AlphaMissense 0.81
- CADD 25.90
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Conflicting classifications of pathogenicity (Hereditary cancer-predisposing syndrome; not specified; Li-Fraum)
- EBI: Likely pathogenic (in sporadic cancers)
- UniProt: Likely pathogenic (in sporadic cancers)
- Most common in the 1KG:CHB population (allele frequency 0.015)
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)
- Cited in: American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. (PMID 17392385)