Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
TCATGTGGTCA/-
Location

Chromosome 1:150646032-150646042 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.150646032_150646042delTCATGTGGTCA

Variation displays