P14S (p.Pro14Ser) variant of SMARCA4 (P51532)
P14S (p.Pro14Ser) in SMARCA4 (P51532) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P14S (p.Pro14Ser) variant details
- p.Pro14Ser
- cosmic curated COSV60812
- ExAC rs754291337
- gnomAD rs754291337
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available