This variation has been flagged

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

Chromosome 22:23315694-23315695 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1042646

This variation has 9 HGVS names - click the plus to show

Variation displays