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:46853826 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981713, CD982927

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7847, 2010_April_001_318_RP2_312600_0004

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

X:g.46853826C>G
ENST00000218340.3:c.453C>G
ENSP00000218340.3:p.Tyr151Ter

Variation displays