Most severe consequence
25
5 prime UTR variant
Alleles
G/C/T|Ancestral: G|Highest population MAF: 0.50
Change tolerance
CADD: C:19.78, T:19.76|GERP: 1.71
Location
Chromosome 8:23246682 (forward strand)|VCF:8 23246682 rs2294123 G C,T
Co-located variant
COSMIC COSV57533033
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Genotyping chips
This variant has assays on 6 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 2 transcripts, has 3009 sample genotypes, is associated with 5 phenotypes and is mentioned in 6 citations.
