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 7:128846396 (forward strand) | View in location tab

Co-located

with COSMIC COSM106745 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000007.12:g.128273686C>T

This variation has 10 HGVS names - click the plus to show

Somatic mutation displays