Most severe consequence
28
intron variant
Alleles
C/G|Ancestral: G|Highest population MAF: 0.46
Change tolerance
CADD: G:0.159|GERP: -3.27
Location
Chromosome 5:112886997 (forward strand)|VCF:5 112886997 rs712662 C G
Co-located variant
COSMIC COSV54840911
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni5
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.
