Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 12:52287296 (forward strand) | View in location tab

Co-located

with COSMIC COSM3998833 (G/A) ; PhenCode HIFD_KRT81:c.1053T>C (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs11170085, rs11552018

This variant has 5 HGVS names - click the plus to show

About this variant

Variant displays