Most severe consequence
28
intron variant
Alleles
C/T|Ancestral: C|Highest population MAF: 0.40
Change tolerance
CADD: T:4.213|GERP: -0.85
Location
Chromosome 5:112890958 (forward strand)|VCF:5 112890958 rs818425 C T
Co-located variant
COSMIC COSV54840964
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
This variant has 3 synonyms - 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 1 transcript and has 3009 sample genotypes.
