This variation has been flagged

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

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

Chromosome 11: between 112095868 and 112095869 (forward strand) | View in location tab


with dbSNP rs369831603 (-/T)

Most severe consequence

This variation has 11 HGVS names - click the plus to show

Variation displays