This variation has been flagged

  • None of the variant alleles match the reference allele (CA)
  • 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]

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

Chromosome 15:74719299-74719300 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name


About this variant

This variant overlaps 20 transcripts.

Variation displays