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 144)|View in dbSNP

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

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

Most severe consequence
Intron variant
HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and 1 regulatory feature.

Variant displays