Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:153993740 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980559

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

X:g.153993740T>G
ENST00000437719.1:c.62T>G
ENSP00000395693.1:p.Phe22Val
ENST00000473552.1:n.159T>G
ENST00000369550.5:c.106T>G
ENSP00000358563.5:p.Phe36Val
ENST00000452771.1:c.64T>G
ENSP00000407325.1:p.Phe22Val
ENST00000413910.1:c.106T>G
ENSP00000400542.1:p.Phe36Val
LRG_55:g.7710T>G
LRG_55t1.1:c.106T>G
LRG_55p1.1:p.Phe36Val

Variation displays