This variant has been flagged

  • None of the variant alleles match the reference allele (CA)
  • 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 (CA) at this location.

Chromosome 1:155296219-155296220 (forward strand)|View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays