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 18:52921925 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM072074

Most severe consequence
Clinical significance

Synonyms

LSDB 10928

This variation has 47 HGVS names - click the plus to show

18:g.52921925G>A
ENST00000570177.2:c.763C>T
ENSP00000454647.1:p.Arg255Ter
ENST00000568740.1:c.1078C>T
ENSP00000455346.1:p.Arg360Ter
ENST00000565018.2:c.1153C>T
ENSP00000455984.1:p.Arg385Ter
ENST00000566279.1:c.973C>T
ENSP00000456125.1:p.Arg325Ter
ENST00000568673.1:c.1081C>T
ENSP00000455135.1:p.Arg361Ter
ENST00000537578.1:c.1081C>T
ENSP00000440731.1:p.Arg361Ter
ENST00000544241.2:c.940C>T
ENSP00000441562.2:p.Arg314Ter
ENST00000562680.1:n.873C>T
ENST00000398339.1:c.1459C>T
ENSP00000381382.1:p.Arg487Ter
ENST00000564403.2:c.1171C>T
ENSP00000457263.1:p.Arg391Ter
ENST00000543082.1:c.1027C>T
ENSP00000439656.1:p.Arg343Ter
ENST00000570287.2:c.673C>T
ENSP00000455763.1:p.Arg225Ter
ENST00000566286.1:c.1144C>T
ENSP00000455418.2:p.Arg382Ter
ENST00000537856.3:c.763C>T
ENSP00000439827.2:p.Arg255Ter
ENST00000564228.1:c.940C>T
ENSP00000455261.1:p.Arg314Ter
ENST00000567880.1:c.973C>T
ENSP00000454366.1:p.Arg325Ter
ENST00000354452.3:c.1153C>T
ENSP00000346440.3:p.Arg385Ter
ENST00000540999.1:c.1081C>T
ENSP00000445202.1:p.Arg361Ter
ENST00000561831.3:c.673C>T
ENSP00000457765.1:p.Arg225Ter
ENST00000563760.1:n.661C>T
ENST00000564999.1:c.1153C>T
ENSP00000457649.1:p.Arg385Ter
ENST00000457482.3:c.673C>T
ENSP00000409447.2:p.Arg225Ter
ENST00000356073.4:c.1153C>T
ENSP00000348374.4:p.Arg385Ter
ENST00000561992.1:c.763C>T
ENSP00000455179.1:p.Arg255Ter

Variation displays