Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.21 (C)

Chromosome 3:133768114 (forward strand) | View in location tab


with COSMIC COSM3759770 (G/C)

Most severe consequence
Synonymous variant
Evidence status


This variant has 4 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2541 sample genotypes and is mentioned in 1 citation.

Variant displays