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

Chromosome 6: between 143946045 and 143946046 (forward strand) | View in location tab


with dbSNP rs3216584 (-/G)

Most severe consequence
Evidence status


Archive dbSNP rs11414469

This variation has 33 HGVS names - click the plus to show

About this variant

This variant overlaps 38 transcripts.

Variation displays