This variation has been flagged

  • None of the variant alleles match the reference allele (AG)
  • 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

A/G | Ambiguity code: R
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (AG) at this location.

Chromosome X:120426651-120426652 (forward strand) | View in location tab

Most severe consequence
HGVS name


Variation displays