Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:111410166 (forward strand) | View in location tab

Co-located

with COSMIC COSM1113201 (C/T), COSM1598660 (C/T) ; HGMD-PUBLIC CM990468, CM980522

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6814, 2010_April_001_066_DCX_300121_0011

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

X:g.111410166C>T
ENST00000371993.4:c.233G>A
ENSP00000361061.2:p.Arg78His
ENST00000468911.1:c.233G>A
ENSP00000418811.1:p.Arg78His
ENST00000496551.1:n.473G>A
ENST00000338081.5:c.476G>A
ENSP00000337697.3:p.Arg159His
ENST00000356220.5:c.233G>A
ENSP00000348553.3:p.Arg78His
ENST00000358070.6:c.451G>A
ENSP00000350776.4:p.Arg151His
ENST00000488120.1:c.233G>A
ENSP00000419861.1:p.Arg78His

Variation displays