Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 10:87957915 (forward strand)|View in location tab

Co-located variants

COSMIC COSM69004, COSM5154, COSM33990, COSM13457 ; HGMD-PUBLIC CM971277

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB Cosmic:5154, 10468

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and is associated with 5 phenotypes.

Variant displays