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
T/C|Ambiguity code: Y
Location

This variant maps to 3 genomic locations; None selected

Evidence status

HGVS name

None

Variant displays