This variation has been flagged

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

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 15:74719513-74719514 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

15:g.74719513_74719514delTCinsT

Variation displays