This variation has been flagged

  • None of the variant alleles match the reference allele
  • Mapped position is not compatible with reported alleles
Select a location:
Original source

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

Alleles
A/G | Ambiguity code: R
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms

Uniprot VAR_033394

HGVS name

None

Variation displays