Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome X:154765478 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980560

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

X:g.154765478C>G
ENST00000437719.3:c.75C>G
ENSP00000395693.1:p.Pro26Arg
ENST00000473552.1:n.172C>G
ENST00000620277.2:c.119C>G
ENSP00000478387.1:p.Pro40Arg
ENST00000369550.7:c.119C>G
ENSP00000358563.5:p.Pro40Arg
ENST00000452771.3:c.77C>G
ENSP00000407325.1:p.Pro26Arg
ENST00000413910.3:c.119C>G
ENSP00000400542.1:p.Pro40Arg
LRG_55:g.7723C>G
LRG_55t1:c.119C>G
LRG_55p1:p.Pro40Arg

Variation displays