Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.20 (G)
Location

Chromosome 12:48145699 (forward strand) | View in location tab

Co-located

with COSMIC COSM3753261 (T/G), COSM3753260 (T/G)

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 8 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 28 transcripts and has 3781 sample genotypes.

Variant displays