S13S (p.Ser13Ser) variant of CALCB (P10092)
S13S (p.Ser13Ser) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
S13S (p.Ser13Ser) variant details
- p.Ser13Ser
- rs1850378038
- gnomAD 11-15074757-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.387
- CADD 15.40
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available