This variant has been flagged

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

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 22:31952035-31952036 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and 1 regulatory feature.

Variant displays