Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 11:112061088 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM052847

Most severe consequence
Clinical significance

Synonyms

LSDB 15920

This variation has 9 HGVS names - click the plus to show

11:g.112061088C>A
ENST00000533297.1:c.*1403C>A
ENST00000527231.1:n.122C>A
ENST00000393051.3:c.1413C>A
ENSP00000376771.1:p.Phe471Leu
ENST00000280346.8:c.1728C>A
ENSP00000280346.6:p.Phe576Leu
ENST00000531306.1:c.1224C>A
ENSP00000433432.1:p.Phe408Leu

Variation displays