This variant has been flagged

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

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

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

Chromosome 12: between 32863450 and 32863451 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17064629

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 1 sample genotype.

Variant displays