This variation has been flagged

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

CTAT/- | Ancestral: T
Note: The reference base for this variant (CTAT) does not match the Ensembl reference base (T) at this location.

Chromosome 6:52476761 (forward strand) | View in location tab

Most severe consequence

This variation has 7 HGVS names - click the plus to show

Variation displays