This variation has been flagged

  • None of the variant alleles match the reference allele (GTTT)
  • Mapped position is not compatible with reported alleles
Original source

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

Alleles
G/T | Ambiguity code: K
Note: The reference sequence for this variant (G) does not match the Ensembl reference sequence (GTTT) at this location.
Location

Chromosome 21:27260001-27260004 (forward strand) | View in location tab

Most severe consequence

This variation has 21 HGVS names - click the plus to show

Variation displays