Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 16:46662452 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4426230 ; HGMD-PUBLIC CM115587

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_018206.4:c.1858G>A

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays