Most severe consequence
28
intron variant
Alleles
G/C|Ancestral: G|Highest population MAF: 0.39
Change tolerance
CADD: C:5.487|GERP: -0.54
Location
Chromosome 5:112889255 (forward strand)|VCF:5 112889255 rs456313 G C
Co-located variant
COSMIC COSV54840952
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
This variant has 2 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.
