Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:101358330 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940192 ; PhenCode BTKbase_U78027.1:g.63145A>G (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

X:g.101358330T>C
ENST00000618050.2:c.1082A>G
ENSP00000479125.1:p.Tyr361Cys
ENST00000372880.3:c.1038+44A>G
ENST00000470329.1:n.32A>G
ENST00000308731.7:c.1082A>G
ENSP00000308176.7:p.Tyr361Cys
ENST00000621635.2:c.1184A>G
ENSP00000483570.1:p.Tyr395Cys
LRG_128:g.32895A>G
LRG_128t1:c.1082A>G
LRG_128p1:p.Tyr361Cys

Variation displays