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 5:142662279 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014594

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2197, 2010_April_001_054_NR3C1_138040_0014

This variation has 19 HGVS names - click the plus to show

5:g.142662279C>T
ENST00000394464.2:c.2035G>A
ENSP00000377977.2:p.Gly679Ser
ENST00000231509.3:c.2038G>A
ENSP00000231509.3:p.Gly680Ser
ENST00000503201.1:c.2035G>A
ENSP00000427672.1:p.Gly679Ser
ENST00000504572.1:c.2038G>A
ENSP00000422518.1:p.Gly680Ser
ENST00000424646.2:c.1957G>A
ENSP00000405282.2:p.Gly653Ser
ENST00000343796.2:c.2035G>A
ENSP00000343205.2:p.Gly679Ser
ENST00000416954.2:c.844G>A
ENSP00000404218.2:p.Gly282Ser
ENST00000415690.2:c.2035G>A
ENSP00000387672.2:p.Gly679Ser
ENST00000394466.2:c.2038G>A
ENSP00000377979.2:p.Gly680Ser

Variation displays