Original source

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

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

Chromosome X:110653443 (forward strand) | View in location tab

Co-located

with COSMIC COSM1145499 (C/T), COSM610407 (C/T) ; HGMD-PUBLIC CM980521

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6804, 2010_April_001_061_DCX_300121_0001

This variation has 16 HGVS names - click the plus to show

X:g.110653443C>T
ENST00000468911.1:c.184G>A
ENSP00000418811.1:p.Asp62Asn
ENST00000496551.1:n.424G>A
ENST00000356220.3:c.184G>A
ENSP00000348553.3:p.Asp62Asn
ENST00000338081.3:c.427G>A
ENSP00000337697.3:p.Asp143Asn
ENST00000358070.4:c.402G>A
ENSP00000350776.4:p.Asp135Asn
ENST00000371993.2:c.184G>A
ENSP00000361061.2:p.Asp62Asn
ENST00000356915.2:c.184G>A
ENSP00000349385.2:p.Asp62Asn
ENST00000488120.1:c.184G>A
ENSP00000419861.1:p.Asp62Asn

Variation displays