Original source

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

G/- | Ancestral: G

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


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

About this variant

This variant overlaps 4 transcripts, has 2 individual genotypes and is associated with 1 phenotype.

Variation displays