This variant has been flagged

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

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 20:9346029-9346037 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

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

About this variant

This variant overlaps 12 transcripts.

Variant displays