Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 4:54285937 (forward strand) | View in location tab

Co-located

with COSMIC COSM12399 (G/T) ; HGMD-PUBLIC CM043866

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:12399, 4749

This variation has 8 HGVS names - click the plus to show

Variation displays