This variation has been flagged

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

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

AAAAA/AAAA/- | Ancestral: A
Note: The reference base for this variant (AAAAA) does not match the Ensembl reference base (A) at this location.

Chromosome 22:50584350 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs71664121, rs71758928

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 48 transcripts.

Variation displays