P11Q (p.Pro11Gln) variant of TTN (Titin)
P11Q (p.Pro11Gln) in TTN (Titin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P11Q (p.Pro11Gln) variant details
- p.Pro11Gln
- NCI-TCGA Cosmic COSV5999
- NCI-TCGA Cosmic COSV6038
- cosmic curated COSV60382
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.