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 14:23431468 (forward strand) | View in location tab

Co-located

with COSMIC COSM954783 (C/T) ; HGMD-PUBLIC CM910268 ; PhenCode FHC0111 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variation displays