Original source

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

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

Chromosome X:46853731 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991106

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7851, 2010_April_001_320_RP2_312600_0008

This variation has 3 HGVS names - click the plus to show

X:g.46853731C>T
ENST00000218340.3:c.358C>T
ENSP00000218340.3:p.Arg120Ter

Variation displays