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]

Alleles
-/GGC/GGCCTGGGCCTG | Ancestral: G
Location

Chromosome 20:2652758 (forward strand) | View in location tab

Co-located

with dbSNP rs6115307 (C/G)

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs68063608

This variation has 17 HGVS names - click the plus to show

Variant allele -
ENST00000329276.7:c.4-84delC
ENST00000445139.1:c.4-84delC
ENST00000494697.3:n.33-84delC
ENST00000469588.3:n.113delC
ENST00000470143.1:n.32-84delC

Variant allele GGC
20:g.2652758delCinsGGC
ENST00000329276.7:c.4-83delGinsGCG
ENST00000445139.1:c.4-83delGinsGCG
ENST00000494697.3:n.33-83delGinsGCG
ENST00000469588.3:n.114delGinsGCG
ENST00000470143.1:n.32-83delGinsGCG

Variant allele GGCCTGGGCCTG
20:g.2652758delCinsGGCCTGGGCCTG
ENST00000329276.7:c.4-83delGinsGCCTGGGCCTGG
ENST00000445139.1:c.4-83delGinsGCCTGGGCCTGG
ENST00000494697.3:n.33-83delGinsGCCTGGGCCTGG
ENST00000469588.3:n.114delGinsGCCTGGGCCTGG
ENST00000470143.1:n.32-83delGinsGCCTGGGCCTGG

Variation displays