This variation has been flagged

  • None of the variant alleles match the reference allele (GCGCGCGCGC)
  • 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]

C/T | Ambiguity code: Y
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (GCGCGCGCGC) at this location.

Chromosome 11:27659649-27659658 (forward strand) | View in location tab


with dbSNP rs202011320 (GCGCGCGCGC/-)

Most severe consequence

Archive dbSNP rs11602143

This variation has 51 HGVS names - click the plus to show

About this variant

This variant overlaps 54 transcripts.

Variation displays