Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 12:114401863 (forward strand) | View in location tab

Co-located

with COSMIC COSM139975 (C/T) ; HGMD-PUBLIC CM971436

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10321, 2010_April_001_121_TBX5_601620_0002

This variation has 10 HGVS names - click the plus to show

Variation displays