This variation has been flagged

  • None of the variant alleles match the reference allele (AC)
  • 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/C | Ambiguity code: M
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (AC) at this location.

Chromosome 22:31952035-31952036 (forward strand) | View in location tab

Most severe consequence

This variation has 13 HGVS names - click the plus to show

Variation displays