This variant has been flagged

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

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 17:27797578-27797579 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays