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 (mapped to GRCh38) (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 1:16986750 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

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

Variation displays