This variation has been flagged

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

Chromosome 8:48922547-48922548 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs2735452

This variation has 2 HGVS names - click the plus to show

Variation displays