This variation has been flagged

  • None of the variant alleles match the reference allele (GT)
  • 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]

C/G | Ambiguity code: S
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (GT) at this location.

Chromosome 13:48232492-48232493 (forward strand) | View in location tab

Most severe consequence
HGVS name


About this variant

This variant overlaps 5 transcripts.

Variation displays