Original source

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

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

Chromosome 5:60186791 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950261

Most severe consequence
Clinical significance

Synonyms

LSDB 16308

This variation has 12 HGVS names - click the plus to show

5:g.60186791G>T
ENST00000426742.2:c.792C>A
ENSP00000400110.2:p.Tyr264Ter
ENST00000265038.5:c.966C>A
ENSP00000265038.5:p.Tyr322Ter
ENST00000462279.1:n.2418C>A
ENST00000381118.3:c.*1010C>A
ENST00000543101.1:c.507C>A
ENSP00000441732.1:p.Tyr169Ter
LRG_466:g.59115C>A
LRG_466t1.1:c.966C>A
LRG_466p1.1:p.Tyr322Ter

Variation displays