This variation has been flagged

  • None of the variant alleles match the reference allele (GC)
  • Mapped position is not compatible with reported alleles
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 4:74847682-74847683 (forward strand) | View in location tab

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Variation displays