This variation has been flagged

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

A/T | Ambiguity code: W
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence () at this location.

Chromosome 10: between 112956367 and 112956368 (forward strand) | View in location tab


with dbSNP rs375394098 (-/A)

Most severe consequence
Evidence status


Archive dbSNP rs59806607

This variation has 31 HGVS names - click the plus to show

About this variant

This variant overlaps 32 transcripts.

Variation displays