This variation has been flagged

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

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

Alleles
CCCAGGGCTCCT/- | Ancestral: C
Note: The reference base for this variant (CCCAGGGCTCCT) does not match the Ensembl reference base (C) at this location.
Location

Chromosome 1:17313245 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

Variation displays