Original source

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

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

Chromosome 11:32392032 (forward strand) | View in location tab

Co-located

with COSMIC COSM21397 (G/A), COSM3397637 (G/A) ; HGMD-PUBLIC CM971596

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14632, 18533

This variant has 19 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature and is associated with 4 phenotypes.

Variant displays