Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 17:4805606 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970306

Most severe consequence
Clinical significance

This variation has 5 HGVS names - click the plus to show

17:g.4805606G>A
ENST00000575637.1:n.71C>T
ENST00000293780.4:c.250C>T
ENSP00000293780.4:p.Arg84Ter
ENST00000381365.3:c.*1778G>A

Variation displays