Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome X:2934870 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030777

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

X:g.2934870G>A
ENST00000545496.3:c.1807C>T
ENSP00000441417.1:p.Pro603Ser
ENST00000540563.3:c.1597C>T
ENSP00000438198.1:p.Pro533Ser
ENST00000381134.5:c.1732C>T
ENSP00000370526.3:p.Pro578Ser

Variation displays