P18Q (p.Pro18Gln) variant of SMARCA4 (P51532)
P18Q (p.Pro18Gln) in SMARCA4 (P51532) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P18Q (p.Pro18Gln) variant details
- p.Pro18Gln
- cosmic curated COSV10075
- Ensembl rs1060502087
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available