Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/- | Ancestral: G

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


with COSMIC COSM1607519 (G/-) ; ClinVar rs730880363 (-/G) ; dbSNP rs555976716 (G/A/C)

Most severe consequence
Splice region variant
Evidence status

Clinical significance

This variant has 7 synonyms - click the plus to show

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

About this variant

This variant overlaps 4 transcripts, has 2 sample genotypes and is associated with 2 phenotypes.

Variant displays