This variation has been flagged

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

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

Chromosome 11:116836621-116836622 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

Variation displays