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 10:87961095 (forward strand)|View in location tab

Co-located variants

COSMIC COSM921156, COSM5151 ; HGMD-PUBLIC CM971278

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5151, 10487

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and is associated with 6 phenotypes.

Variant displays