This variant has been flagged

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

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

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

Chromosome 7:243228-243229 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays