Original source

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

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

Chromosome 5:142680085 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020743

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2193, 2010_April_001_051_NR3C1_138040_0010

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

5:g.142680085A>G
ENST00000394464.2:c.1712T>C
ENSP00000377977.2:p.Val571Ala
ENST00000231509.3:c.1715T>C
ENSP00000231509.3:p.Val572Ala
ENST00000503201.1:c.1712T>C
ENSP00000427672.1:p.Val571Ala
ENST00000504572.1:c.1715T>C
ENSP00000422518.1:p.Val572Ala
ENST00000424646.2:c.1634T>C
ENSP00000405282.2:p.Val545Ala
ENST00000343796.2:c.1712T>C
ENSP00000343205.2:p.Val571Ala
ENST00000416954.2:c.521T>C
ENSP00000404218.2:p.Val174Ala
ENST00000415690.2:c.1712T>C
ENSP00000387672.2:p.Val571Ala
ENST00000394466.2:c.1715T>C
ENSP00000377979.2:p.Val572Ala

Variation displays