Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 15:63044030 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1230147, COSM1230146 ; HGMD-PUBLIC CM014115

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 50 HGVS names - Show

About this variant

This variant overlaps 52 transcripts, 1 regulatory feature, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays