Original source

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

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

Chromosome X:111401121 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980529

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_062_DCX_300121_0002, 6805

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

X:g.111401121G>A
ENST00000371993.4:c.574C>T
ENSP00000361061.2:p.Arg192Trp
ENST00000496551.1:n.814C>T
ENST00000338081.5:c.817C>T
ENSP00000337697.3:p.Arg273Trp
ENST00000356220.5:c.574C>T
ENSP00000348553.3:p.Arg192Trp
ENST00000358070.6:c.792C>T
ENSP00000350776.4:p.Arg265Trp
ENST00000488120.1:c.574C>T
ENSP00000419861.1:p.Arg192Trp

Variation displays