Most severe consequence
22
synonymous variant
Alleles
G/A/C/T|Ancestral: A|Highest population MAF: 0.50
Change tolerance
CADD: A:13.51, C:9.931, T:11.13|GERP: 0.26
Location
Chromosome 5:112828864 (forward strand)|VCF:5 112828864 rs351771 G A,C,T
Co-located variant
COSMIC COSV57321606
Evidence status 
Clinical significance
HGVS names
This variant has 45 HGVS names - Show
Synonyms
This variant has 8 synonyms - Show
Genotyping chips
This variant has assays on 4 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 7 transcripts, has 3009 sample genotypes, is associated with 8 phenotypes and is mentioned in 22 citations.
Description from SNPedia
Description not available [More information from SNPedia]
