This variation has been flagged

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

-/CTCA | Ancestral: C

Chromosome 7:100722528 (forward strand) | View in location tab


with dbSNP rs484199 (C/T)

Most severe consequence
Evidence status


This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1 individual genotype.

Variation displays