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 11:124875581 (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.124875581C>T
ENST00000538940.2:c.2251C>T
ENSP00000441797.1:p.Gln751Ter
ENST00000397801.2:c.2317C>T
ENSP00000380903.1:p.Gln773Ter

Variation displays