Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 14:20472468 (forward strand) | View in location tab

Co-located

with COSMIC COSM2029164 (C/T) ; HGMD-PUBLIC CM012158 ; PhenCode NPbase_D0064:g.4059C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4325, 2010_April_001_040_NP_164050_0009

This variation has 13 HGVS names - click the plus to show

Variation displays