This variant has been flagged

  • None of the variant alleles match the reference allele
  • Mapped position is not compatible with reported alleles
Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

This variant maps to 2 genomic locations; None selected

HGVS name

None

Variant displays