Original source

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

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

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

Co-located

with COSMIC COSM3759770 (G/C)

Most severe consequence
Evidence status

Synonyms

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 2541 individual genotypes and is mentioned in 1 citation.

Variation displays