Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

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

Co-located

with COSMIC COSM3771282 (G/A) ; HGMD-PUBLIC CM023465

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14742

This variant has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and is associated with 3 phenotypes.

Variant displays