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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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