S69N (p.Ser69Asn) variant of TNNC1 (P63316)
S69N (p.Ser69Asn) in TNNC1 (P63316) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
S69N (p.Ser69Asn) variant details
- p.Ser69Asn
- rs1276999572
- gnomAD 19-55156282-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.247
- CADD 13.40
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- Structural context available
- Literature evidence available