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]

-/TTTCT/TTTTC | Ancestral: T

Chromosome 19:48974919 (forward strand) | View in location tab


with dbSNP rs144426771 (T/C)

Most severe consequence
Evidence status


Archive dbSNP rs74389437

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts.

Variation displays