Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 5:142689700 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014593

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_053_NR3C1_138040_0013, 2196

This variation has 20 HGVS names - click the plus to show

5:g.142689700C>T
ENST00000394464.2:c.1430G>A
ENSP00000377977.2:p.Arg477His
ENST00000231509.3:c.1433G>A
ENSP00000231509.3:p.Arg478His
ENST00000503201.1:c.1430G>A
ENSP00000427672.1:p.Arg477His
ENST00000504336.1:n.370G>A
ENST00000504572.1:c.1433G>A
ENSP00000422518.1:p.Arg478His
ENST00000424646.2:c.1352G>A
ENSP00000405282.2:p.Arg451His
ENST00000343796.2:c.1430G>A
ENSP00000343205.2:p.Arg477His
ENST00000416954.2:c.239G>A
ENSP00000404218.2:p.Arg80His
ENST00000415690.2:c.1430G>A
ENSP00000387672.2:p.Arg477His
ENST00000394466.2:c.1433G>A
ENSP00000377979.2:p.Arg478His

Variation displays