Most severe consequence
28
intron variant
Alleles
C/T|Ancestral: C|Highest population MAF: 0.38
Change tolerance
CADD: T:4.363|GERP: -3.54
Location
Chromosome 5:112886172 (forward strand)|VCF:5 112886172 rs818427 C T
Co-located variant
COSMIC COSV54840900
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, has 3009 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.
