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 8:89958760 (forward strand)|View in location tab

Co-located variants

COSMIC COSM245943 ; HGMD-PUBLIC CM054792

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 4 phenotypes.

Variant displays