Original source

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

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

Chromosome 10:87933148 (forward strand) | View in location tab


with COSMIC COSM5817 (G/-), COSM5033 (G/A), COSM5277 (G/C), COSM5216 (G/T) ; HGMD-PUBLIC CM991081, CM981670 ; dbSNP rs121913292 (G/-)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB Cosmic:5033, 10483

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is associated with 4 phenotypes.

Variant displays