Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:111410260 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980520

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_065_DCX_300121_0007, 6810

This variation has 14 HGVS names - click the plus to show

X:g.111410260T>G
ENST00000371993.4:c.139A>C
ENSP00000361061.2:p.Ser47Arg
ENST00000468911.1:c.139A>C
ENSP00000418811.1:p.Ser47Arg
ENST00000496551.1:n.379A>C
ENST00000338081.5:c.382A>C
ENSP00000337697.3:p.Ser128Arg
ENST00000356220.5:c.139A>C
ENSP00000348553.3:p.Ser47Arg
ENST00000358070.6:c.357A>C
ENSP00000350776.4:p.Ser120Arg
ENST00000488120.1:c.139A>C
ENSP00000419861.1:p.Ser47Arg

Variation displays