Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 1:201359243 (forward strand) | View in location tab


with COSMIC COSM209474 (G/A)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 19 transcripts.

Variant displays