Original source

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

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

Chromosome 2:208248389 (forward strand) | View in location tab

Co-located

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

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 34 HGVS names - click the plus to show

Variation displays