S37N (p.Ser37Asn) variant of SPTA1 (P02549)
S37N (p.Ser37Asn) in SPTA1 (P02549) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data.
S37N (p.Ser37Asn) variant details
- p.Ser37Asn
- cosmic curated COSV10746
- TOPMed rs1188198052
- gnomAD rs1188198052
- Missense
- Variant Prioritization Score for Impact Estimate 0.309
- CADD 15.10
- PolyPhen-2 0.00
- SIFT 0.15
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)