Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5033, 10483

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

Variation displays