Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 12:6537154 (forward strand) | View in location tab

Co-located

with COSMIC COSM3998914 (T/C)

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts and has 2526 sample genotypes.

Variant displays