Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 4:54285926 (forward strand) | View in location tab

Co-located

with COSMIC COSM736 (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4741, Cosmic:736

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

4:g.54285926A>T
ENST00000507166.3:c.1805A>T
ENSP00000423325.1:p.Asp602Val
ENST00000257290.7:c.2525A>T
ENSP00000257290.5:p.Asp842Val
LRG_309:g.61830A>T
LRG_309t1:c.2525A>T
LRG_309p1:p.Asp842Val

Variation displays