Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 10:89692905 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5033, 10483

This variation has 7 HGVS names - click the plus to show

Variation displays