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 11:124745477 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061187

Most severe consequence
Clinical significance

Synonyms

LSDB 15861

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

11:g.124745477C>T
ENST00000397801.1:c.2317C>T
ENSP00000380903.1:p.Gln773Ter
ENST00000538940.1:c.2251C>T
ENSP00000441797.1:p.Gln751Ter

Variation displays