Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 12:49272399 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3359770

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3175478

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2505 sample genotypes.

Variant displays