V13M (p.Val13Met) variant of BRIP1 (Fanconi anemia group J protein)
V13M (p.Val13Met) in BRIP1 (Fanconi anemia group J protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Familial cancer of breast; Fanconi anem. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data, published literature, and structural context.
V13M (p.Val13Met) variant details
- p.Val13Met
- rs1488264110
- ClinGen CA400486024
- ClinVar RCV001976253
- ClinVar RCV002361334
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Familial cancer of breast; Fanconi anem
- Missense
- Variant Prioritization Score for Impact Estimate 0.538
- REVEL 0.40
- AlphaMissense 0.53
- MetaLR 0.32
- MetaSVM -0.51
- CADD 25.00
- PolyPhen-2 0.97
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Familial cancer of brea)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Cited in: Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. (PMID 15604628)
- Cited in: Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National… (PMID 17508274)