This variation has been flagged

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

AT/- | Ancestral: T
Note: The reference base for this variant (AT) does not match the Ensembl reference base (T) at this location.

Chromosome 1:91712124 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 89 individual genotypes.

Variation displays