Original source

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

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

Chromosome 3:165786255 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920126

Most severe consequence
Clinical significance

Synonyms

LSDB 5069

This variation has 10 HGVS names - click the plus to show

3:g.165786255T>A
ENST00000482958.1:c.*80A>T
ENST00000264381.5:c.1574A>T
ENSP00000264381.3:p.Glu525Val
ENST00000479451.3:c.164A>T
ENSP00000418325.1:p.Glu55Val
ENST00000488954.1:c.164A>T
ENSP00000418504.1:p.Glu55Val
ENST00000497011.3:c.1574A>T
ENSP00000419505.1:p.Glu525Val

Variation displays