Original source

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

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

Chromosome 18:52752126 (forward strand) | View in location tab

Co-located

with COSMIC COSM106533 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000018.8:g.48532494G>A

This variation has 7 HGVS names - click the plus to show

Somatic mutation displays