Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 12:52316525 (forward strand) | View in location tab

Co-located

with COSMIC COSM147523 (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs58145116

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2512 sample genotypes.

Variant displays