Original source

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

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

Chromosome X:10535245 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004766

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_245_MID1_300552_0005, 7588

This variation has 19 HGVS names - click the plus to show

X:g.10535245C>A
ENST00000413894.1:c.343G>T
ENSP00000391154.1:p.Glu115Ter
ENST00000380780.1:c.343G>T
ENSP00000370157.1:p.Glu115Ter
ENST00000380779.1:c.343G>T
ENSP00000370156.1:p.Glu115Ter
ENST00000380787.1:c.343G>T
ENSP00000370164.1:p.Glu115Ter
ENST00000453318.2:c.343G>T
ENSP00000414521.2:p.Glu115Ter
ENST00000423614.1:c.343G>T
ENSP00000387771.1:p.Glu115Ter
ENST00000380782.2:c.343G>T
ENSP00000370159.1:p.Glu115Ter
ENST00000380785.1:c.343G>T
ENSP00000370162.1:p.Glu115Ter
ENST00000317552.4:c.343G>T
ENSP00000312678.4:p.Glu115Ter

Variation displays