This variation maps to 6 locations

Select a location:
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

This variation maps to 6 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NC_000006.10:g.32890114C>T

HGVS name

None

Somatic mutation displays