Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 5:143300520 (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 17 HGVS names - click the plus to show

5:g.143300520A>G
ENST00000394464.3:c.1712T>C
ENSP00000377977.2:p.Val571Ala
ENST00000231509.4:c.1715T>C
ENSP00000231509.3:p.Val572Ala
ENST00000504572.2:c.1715T>C
ENSP00000422518.1:p.Val572Ala
ENST00000503201.1:c.1712T>C
ENSP00000427672.1:p.Val571Ala
ENST00000424646.3:c.1634T>C
ENSP00000405282.2:p.Val545Ala
ENST00000343796.3:c.1712T>C
ENSP00000343205.2:p.Val571Ala
ENST00000415690.3:c.1712T>C
ENSP00000387672.2:p.Val571Ala
ENST00000394466.3:c.1715T>C
ENSP00000377979.2:p.Val572Ala

Variation displays