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

Co-located

with COSMIC COSM1628449 (G/A) ; HGMD-PUBLIC CM065059

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_039_CDKN1B_600778_0001, 9523

This variant has 7 HGVS names - click the plus to show

About this variant

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

Variant displays