This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

This variant maps to 6 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NC_000006.10:g.32890114C>T

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and is mentioned in 1 citation.

Somatic mutation displays