Most severe consequence
28
intron variant
Alleles
COSMIC_MUTATION|Ancestral: C
Location
Chromosome 11:168187 (forward strand)|VCF:11 168187 COSV68417205 C N
Co-located variant
dbSNP rs1354132918 (C/G/T)
Evidence status 
Original source
Somatic mutations found in human cancers from the COSMIC catalogue (release 98)|View in COSMIC
About this variant
This variant has predicted consequences for 2 transcripts and is associated with 1 phenotype.
