M18V (p.Met18Val) variant of BRCA1 (P38398)
M18V (p.Met18Val) in BRCA1 (P38398) is a missense change. Clinical records from EBI and UniProt describe it as likely benign in the context of in BC. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes experimental measurements, published literature, and structural context.
M18V (p.Met18Val) variant details
- p.Met18Val
- rs2055727017
- ClinGen CA10602054
- ClinVar RCV001072373
- ClinVar RCV001264576
- Likely benign
- in BC
- Missense
- Variant Prioritization Score for Impact Estimate 0.499
- AlphaMissense 0.47
- MetaLR 0.39
- MetaSVM -0.16
- PolyPhen-2 0.03
- SIFT 0.28
- EVE 0.72
- EBI: Likely benign (in BC)
- UniProt: Likely benign (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)