Most severe consequence
28
intron variant
Alleles
COSMIC_MUTATION|Ancestral: C
Change tolerance
GERP: -0.85
Location
Chromosome 5:112890958 (forward strand)|VCF:5 112890958 COSV54840964 C N
Co-located variant
dbSNP rs818425 (C/T)
Evidence status 
Original source
Somatic mutations found in human cancers from the COSMIC catalogue (release 102)|View in COSMIC
About this variant
This variant has predicted consequences for 1 transcript and is associated with 1 phenotype.
