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:101353935 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

X:g.101353935C>G
ENST00000618050.1:c.1685G>C
ENSP00000479125.1:p.Arg562Pro
ENST00000470069.1:n.50G>C
ENST00000488970.1:n.287G>C
ENST00000372880.2:c.1157G>C
ENSP00000361971.1:p.Arg386Pro
ENST00000308731.7:c.1685G>C
ENSP00000308176.7:p.Arg562Pro
ENST00000621635.1:c.1787G>C
ENSP00000483570.1:p.Arg596Pro
LRG_128:g.37290G>C
LRG_128t1.1:c.1685G>C
LRG_128p1.1:p.Arg562Pro

Variation displays