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 11:6617040 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3718418 ; HGMD-PUBLIC CM970326

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 15415

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and is associated with 3 phenotypes.

Variant displays