Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 8:19951916 (forward strand)|View in location tab

Co-located variants

COSMIC COSM39324 ; HGMD-PUBLIC CM900160

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 16457

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays