R7C (p.Arg7Cys) variant of BRCA1 (P38398)
R7C (p.Arg7Cys) in BRCA1 (P38398) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
R7C (p.Arg7Cys) variant details
- p.Arg7Cys
- rs80356994
- ClinGen CA001330
- cosmic curated COSV10052
- ClinVar RCV000031021
- Likely benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.519
- REVEL 0.56
- AlphaMissense 0.24
- MetaLR 0.40
- MetaSVM -0.50
- CADD 24.40
- PolyPhen-2 0.21
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- BRCA1 SGE Exon 2 Replicate 2: score -1.33
- 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)