This variant has been flagged

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

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

G/T | Ambiguity code: K
Note: The reference sequence for this variant (G) does not match the Ensembl reference sequence (GTTT) at this location.

Chromosome 21:25887689-25887692 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 19 HGVS names - Show

About this variant

This variant overlaps 18 transcripts.

Variant displays