Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 5:132659419 (forward strand) | View in location tab

Co-located

with COSMIC COSM109445 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000005.8:g.132023010C>T

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

Somatic mutation displays