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 11:44275472 (forward strand) | View in location tab

Co-located

with COSMIC COSM188962 (C/T) ; HGMD-PUBLIC CM010011

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_007_ALX4_605420_0003, NP_068745.2:p.Arg218Gln, 13161

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

Variation displays