Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.06 (G)
Location

Chromosome 2:236167453 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749638 (C/G)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 6 transcripts and has 2504 individual genotypes.

Variation displays