Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

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

Co-located

with COSMIC COSM245943 (G/A) ; HGMD-PUBLIC CM054792

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 11344

This variant has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is associated with 3 phenotypes.

Variant displays