This variation has been flagged

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

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

Alleles
AT/- | Ancestral: A
Note: The reference base for this variant (AT) does not match the Ensembl reference base (A) at this location.
Location

Chromosome 10:54529677 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

Variation displays