Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 14:23429005 (forward strand) | View in location tab

Co-located

with COSMIC COSM2031862 (G/A) ; HGMD-PUBLIC CM087715, CM920490 ; PhenCode FHC0121 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 29168, 4195

This variation has 12 HGVS names - click the plus to show

Variation displays