This variation has been flagged

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

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

A/C | Ambiguity code: M

This variation maps to 2 genomic locations; None selected

HGVS name


About this variant

This variant overlaps 1 transcript.

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