This variation has been flagged

  • None of the variant alleles match the reference allele (GC)
  • 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

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

Chromosome 1:153259680-153259681 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs762577

HGVS name

1:g.153259680_153259681delGCinsG

Variation displays