Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:124739931 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061188

Most severe consequence
Clinical significance

Synonyms

LSDB 15860

This variation has 5 HGVS names - click the plus to show

11:g.124739931C>T
ENST00000538940.1:c.667C>T
ENSP00000441797.1:p.Arg223Trp
ENST00000397801.1:c.733C>T
ENSP00000380903.1:p.Arg245Trp

Variation displays