Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 2:209113113 (forward strand) | View in location tab


with COSMIC COSM28747 (G/A), COSM28749 (G/C), COSM28748 (G/T)

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 20 HGVS names - click the plus to show

Variation displays