Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 16:88651007 (forward strand) | View in location tab

Co-located

with COSMIC COSM131493 (G/A) ; HGMD-PUBLIC CM001111 ; PhenCode CYBAbase_D0024:g.1035C>T (G/A)

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_029_CYBA_608508_0009, 15775

This variant has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays