Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V
Location

Chromosome 17:17215228 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3771282 ; HGMD-PUBLIC CM023465

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14742

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 3 phenotypes.

Variant displays