Original source

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

Alleles
CT/TA/TCT/TTA
Location

Chromosome X:154765949-154765950 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_006814

This variation has 45 HGVS names - click the plus to show

Variant allele TCT
X:g.154765949_154765950delCTinsTCT
ENST00000437719.2:c.170_171delCTinsTCT
ENSP00000395693.1:p.Leu58SerfsTer22
ENST00000473552.1:n.267_268delCTinsTCT
ENST00000620277.1:c.214_215delCTinsTCT
ENSP00000478387.1:p.Leu72SerfsTer22
ENST00000369550.6:c.214_215delCTinsTCT
ENSP00000358563.5:p.Leu72SerfsTer22
ENST00000452771.2:c.172_173delCTinsTCT
ENSP00000407325.1:p.Leu58SerfsTer22
ENST00000413910.2:c.214_215delCTinsTCT
ENSP00000400542.1:p.Leu72SerfsTer22
LRG_55:g.8194_8195delCTinsTCT
LRG_55t1.1:c.214_215delCTinsTCT
LRG_55p1.1:p.Leu72SerfsTer22

Variant allele TA
X:g.154765949_154765950delCTinsTA
ENST00000437719.2:c.170_171delCTinsTA
ENSP00000395693.1:p.Leu58Tyr
ENST00000473552.1:n.267_268delCTinsTA
ENST00000620277.1:c.214_215delCTinsTA
ENSP00000478387.1:p.Leu72Tyr
ENST00000369550.6:c.214_215delCTinsTA
ENSP00000358563.5:p.Leu72Tyr
ENST00000452771.2:c.172_173delCTinsTA
ENSP00000407325.1:p.Leu58Tyr
ENST00000413910.2:c.214_215delCTinsTA
ENSP00000400542.1:p.Leu72Tyr
LRG_55:g.8194_8195delCTinsTA
LRG_55t1.1:c.214_215delCTinsTA
LRG_55p1.1:p.Leu72Tyr

Variant allele TTA
X:g.154765949_154765950delCTinsTTA
ENST00000437719.2:c.170_171delCTinsTTA
ENSP00000395693.1:p.Ala59CysfsTer21
ENST00000473552.1:n.267_268delCTinsTTA
ENST00000620277.1:c.214_215delCTinsTTA
ENSP00000478387.1:p.Ala73CysfsTer21
ENST00000369550.6:c.214_215delCTinsTTA
ENSP00000358563.5:p.Ala73CysfsTer21
ENST00000452771.2:c.172_173delCTinsTTA
ENSP00000407325.1:p.Ala59CysfsTer21
ENST00000413910.2:c.214_215delCTinsTTA
ENSP00000400542.1:p.Ala73CysfsTer21
LRG_55:g.8194_8195delCTinsTTA
LRG_55t1.1:c.214_215delCTinsTTA
LRG_55p1.1:p.Ala73CysfsTer21

Variation displays