Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
CT/TA
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 15 HGVS names - click the plus to show

X:g.154765949_154765950delCTinsTA
ENST00000437719.4:c.170_171delCTinsTA
ENSP00000395693.1:p.Leu58Tyr
ENST00000473552.1:n.267_268delCTinsTA
ENST00000620277.3:c.214_215delCTinsTA
ENSP00000478387.1:p.Leu72Tyr
ENST00000369550.8:c.214_215delCTinsTA
ENSP00000358563.5:p.Leu72Tyr
ENST00000452771.4:c.172_173delCTinsTA
ENSP00000407325.1:p.Leu58Tyr
ENST00000413910.4:c.214_215delCTinsTA
ENSP00000400542.1:p.Leu72Tyr
LRG_55:g.8194_8195delCTinsTA
LRG_55t1:c.214_215delCTinsTA
LRG_55p1:p.Leu72Tyr

About this variant

This variant overlaps 14 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays