V9M (p.Val9Met) variant of KMT2C (Q8NEZ4)
V9M (p.Val9Met) in KMT2C (Q8NEZ4) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and population frequency data.
V9M (p.Val9Met) variant details
- p.Val9Met
- NCI-TCGA Cosmic COSV1000
- cosmic curated COSV10007
- NCI-TCGA Cosmic COSV5152
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.26
- CADD 19.50
- PolyPhen-2 0.02
- SIFT 0.06
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9.6e-07)