Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 4:54285937 (forward strand) | View in location tab

Co-located

with COSMIC COSM12399 (G/T) ; HGMD-PUBLIC CM043866

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:12399, 4749

This variation has 8 HGVS names - click the plus to show

4:g.54285937G>T
ENST00000507166.3:c.1816G>T
ENSP00000423325.1:p.Asp606Tyr
ENST00000257290.7:c.2536G>T
ENSP00000257290.5:p.Asp846Tyr
LRG_309:g.61841G>T
LRG_309t1.1:c.2536G>T
LRG_309p1.1:p.Asp846Tyr

Variation displays