Original source

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

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

Chromosome 14:23429279 (forward strand) | View in location tab

Co-located

with COSMIC COSM954779 (G/A) ; HGMD-PUBLIC CM930504 ; PhenCode FHC0118 (G/A)

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