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 11:124870035 (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.124870035C>T
ENST00000397801.3:c.733C>T
ENSP00000380903.1:p.Arg245Trp
ENST00000538940.3:c.667C>T
ENSP00000441797.1:p.Arg223Trp

Variation displays