Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/-|Ancestral: G
Location

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

Co-located variants

COSMIC COSM1607519 ; dbSNP rs555976716 (G/A/C/T)

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

Synonyms

This variant has 7 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

About this variant

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

Variant displays