Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.22 (C)

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


with COSMIC COSM3759770 (G/C)

Most severe consequence
Evidence status


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

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

About this variant

This variant overlaps 4 transcripts, has 2022 individual genotypes and is mentioned in 1 citation.

Variation displays