Original source

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

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

Chromosome 9:126693250 (forward strand) | View in location tab

Co-located

with COSMIC COSM1460049 (G/A), COSM1460050 (G/A) ; HGMD-PUBLIC CM981214

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

9:g.126693250G>A
ENST00000373474.5:c.668G>A
ENSP00000362573.3:p.Arg223Gln
ENST00000526117.2:c.668G>A
ENSP00000436930.1:p.Arg223Gln
ENST00000561065.1:c.599G>A
ENSP00000453580.1:p.Arg200Gln
ENST00000355497.6:c.668G>A
ENSP00000347684.5:p.Arg223Gln

Variation displays