Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:6845648 (forward strand) | View in location tab

Co-located

with COSMIC COSM3676525 (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs57580306

This variant has 9 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 21 transcripts and has 89 sample genotypes.

Variant displays