Original source

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

Alleles
G/- | Ancestral: G
Location

Chromosome 14:23389063 (forward strand) | View in location tab

Co-located

with COSMIC COSM1607519 (G/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

Variation displays