Original source

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

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

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

Co-located

with COSMIC COSM5151 (C/T), COSM921156 (C/G) ; HGMD-PUBLIC CM971278

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5151, 10487

This variant has 8 HGVS names - click the plus to show

About this variant

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

Variant displays