Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 12:12871000 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_039_CDKN1B_600778_0001, 9523

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

Variation displays