Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome X:111401087 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980531

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_064_DCX_300121_0006, 6809

This variation has 12 HGVS names - click the plus to show

X:g.111401087G>C
ENST00000371993.4:c.608C>G
ENSP00000361061.2:p.Thr203Arg
ENST00000496551.1:n.848C>G
ENST00000338081.5:c.851C>G
ENSP00000337697.3:p.Thr284Arg
ENST00000356220.5:c.608C>G
ENSP00000348553.3:p.Thr203Arg
ENST00000488120.1:c.608C>G
ENSP00000419861.1:p.Thr203Arg
ENST00000358070.6:c.826C>G
ENSP00000350776.4:p.Thr276Arg

Variation displays