Original source

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

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

Chromosome 5:60200621 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM055940

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

5:g.60200621G>A
ENST00000265038.5:c.479C>T
ENSP00000265038.5:p.Ala160Val
ENST00000495985.1:n.252C>T
ENST00000439176.1:c.305C>T
ENSP00000408344.1:p.Ala102Val
ENST00000543101.1:c.23-1078C>T
ENST00000426742.2:c.305C>T
ENSP00000400110.2:p.Ala102Val
ENST00000497892.1:n.522C>T
ENST00000484330.1:n.227-2286C>T
ENST00000462279.1:n.324C>T
ENST00000381118.3:c.*523C>T
LRG_466:g.45285C>T
LRG_466t1.1:c.479C>T
LRG_466p1.1:p.Ala160Val

Variation displays