M18R (p.Met18Arg) variant of BRCA1 (P38398)
M18R (p.Met18Arg) in BRCA1 (P38398) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic in the context of in BC. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes experimental measurements, published literature, and structural context.
M18R (p.Met18Arg) variant details
- p.Met18Arg
- rs80356929
- ClinGen CA10602052
- ClinVar RCV000637401
- ClinVar RCV001072375
- Pathogenic
- in BC
- Missense
- Variant Prioritization Score for Impact Estimate 0.709
- AlphaMissense 0.97
- MetaLR 0.64
- MetaSVM 0.30
- PolyPhen-2 0.97
- SIFT 0.00
- EVE 0.86
- EBI: Pathogenic (in BC)
- UniProt: Pathogenic (in BC)
- Structural context available
- BRCA1 SGE Exon 2 Replicate 2: score -0.148
- Cited in: Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. (PMID 15604628)
- Cited in: American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. (PMID 17392385)