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:10567205 (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 23 HGVS names - click the plus to show

X:g.10567205C>A
ENST00000610939.1:c.343G>T
ENSP00000483707.1:p.Glu115Ter
ENST00000413894.3:c.343G>T
ENSP00000391154.1:p.Glu115Ter
ENST00000616003.2:c.343G>T
ENSP00000484712.1:p.Glu115Ter
ENST00000380780.3:c.343G>T
ENSP00000370157.1:p.Glu115Ter
ENST00000380779.3:c.343G>T
ENSP00000370156.1:p.Glu115Ter
ENST00000380787.3:c.343G>T
ENSP00000370164.1:p.Glu115Ter
ENST00000423614.1:c.343G>T
ENSP00000387771.1:p.Glu115Ter
ENST00000453318.4:c.343G>T
ENSP00000414521.2:p.Glu115Ter
ENST00000380782.4:c.343G>T
ENSP00000370159.1:p.Glu115Ter
ENST00000380785.3:c.343G>T
ENSP00000370162.1:p.Glu115Ter
ENST00000317552.6:c.343G>T
ENSP00000312678.4:p.Glu115Ter

Variation displays