Original source

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

C/G/T|Ancestral: C|Ambiguity code: B

Chromosome 10:87933147 (forward strand)|View in location tab

Co-located variants
Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 10473, Cosmic:5152, Cosmic:5219

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 6 phenotypes.

Variant displays