Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome X:111410188 (forward strand) | View in location tab

Co-located

with COSMIC COSM319830 (C/G) ; HGMD-PUBLIC CM004409

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_069_DCX_300121_0014, 6817

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

X:g.111410188C>A
ENST00000371993.3:c.211G>T
ENSP00000361061.2:p.Ala71Ser
ENST00000468911.1:c.211G>T
ENSP00000418811.1:p.Ala71Ser
ENST00000496551.1:n.451G>T
ENST00000338081.4:c.454G>T
ENSP00000337697.3:p.Ala152Ser
ENST00000356220.4:c.211G>T
ENSP00000348553.3:p.Ala71Ser
ENST00000488120.1:c.211G>T
ENSP00000419861.1:p.Ala71Ser
ENST00000358070.5:c.429G>T
ENSP00000350776.4:p.Ala144Ser

Variation displays