Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:46728139 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4033078 ; HGMD-PUBLIC CM002958

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4990

HGVS names

This variant has 8 HGVS names - Hide

11:g.46728139G>A
ENST00000530231.5:c.1274G>A
ENSP00000433907.1:p.Arg425His
ENST00000311907.9:c.1274G>A
ENSP00000308541.5:p.Arg425His
LRG_551:g.13947G>A
LRG_551t1:c.1274G>A
LRG_551p1:p.Arg425His

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays