Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 17:21416455 (forward strand) | View in location tab

Co-located

with COSMIC COSM1285668 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000017.9:g.21260360C>G

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

Variation displays