Original source

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

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

Chromosome 5:150073481 (forward strand) | View in location tab

Co-located

with COSMIC COSM946 (A/T), COSM954 (A/G)

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

Variation displays