Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.47 (G)
Location

Chromosome 7:128589427 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR072316

Most severe consequence
Evidence status

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

7:g.128589427G>A
ENST00000249375.4:c.*555G>A
ENST00000465603.1:c.*1580G>A
ENST00000473745.1:c.*555G>A
ENST00000402030.2:c.*555G>A

This variation has assays on 4 chips - click the plus to show

Variation displays