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 12:12718066 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1628449 ; HGMD-PUBLIC CM065059

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_039_CDKN1B_600778_0001, 9523

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays