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 17:39725721 (forward strand) | View in location tab

Co-located

with COSMIC COSM684 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

17:g.39725721G>A
ENST00000583038.3:n.4300G>A
ENST00000584450.3:c.2740G>A
ENSP00000463714.1:p.Glu914Lys
ENST00000541774.3:c.2695G>A
ENSP00000446466.1:p.Glu899Lys
ENST00000445658.4:c.1912G>A
ENSP00000404047.2:p.Glu638Lys
ENST00000269571.7:c.2740G>A
ENSP00000269571.4:p.Glu914Lys
ENST00000406381.4:c.2650G>A
ENSP00000385185.2:p.Glu884Lys
ENST00000578373.3:c.*2530G>A
ENST00000584601.3:c.2650G>A
ENSP00000462438.1:p.Glu884Lys

Variation displays