Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome X:147018053 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930253

Most severe consequence
Clinical significance

Synonyms

LSDB 8374

This variation has 15 HGVS names - click the plus to show

X:g.147018053T>A
ENST00000440235.2:c.-86T>A
ENST00000218200.8:c.911T>A
ENSP00000218200.8:p.Ile304Asn
ENST00000370475.4:c.911T>A
ENSP00000359506.4:p.Ile304Asn
ENST00000370471.3:c.911T>A
ENSP00000359502.3:p.Ile304Asn
ENST00000370470.1:c.911T>A
ENSP00000359501.1:p.Ile304Asn
ENST00000439526.2:c.905T>A
ENSP00000395923.2:p.Ile302Asn
ENST00000370477.1:c.911T>A
ENSP00000359508.1:p.Ile304Asn
ENST00000475038.1:n.221T>A

Variation displays