This variant has been flagged

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

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

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

Chromosome 8:48922547-48922548 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant

Archive dbSNP rs2735452

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays