P2S (p.Pro2Ser) variant of SLC22A1 (O15245)
P2S (p.Pro2Ser) in SLC22A1 (O15245) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P2S (p.Pro2Ser) variant details
- p.Pro2Ser
- NCI-TCGA Cosmic COSV6145
- cosmic curated COSV61452
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available