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 4:154586358 (forward strand) | View in location tab

Co-located

with COSMIC COSM3601166 (G/T), COSM3601165 (G/T)

Most severe consequence
Evidence status

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

Variation displays