Q12P (p.Gln12Pro) variant of BRCA1 (P38398)
Q12P (p.Gln12Pro) in BRCA1 (P38398) is a missense change. Clinical records from EBI and UniProt describe it as likely pathogenic. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
Q12P (p.Gln12Pro) variant details
- p.Gln12Pro
- rs1555601006
- ClinGen CA10602093
- ClinVar RCV001076454
- ClinVar RCV001351289
- Likely pathogenic
- Missense
- Variant Prioritization Score for Impact Estimate 0.618
- REVEL 0.67
- ESM-1b 1.00
- AlphaMissense 0.75
- MetaLR 0.51
- MetaSVM 0.04
- CADD 24.30
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Enrich2 nucleotide variant scores for BRCA1 E3: score -0.218
- 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)