Original source

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

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

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

Co-located

with COSMIC COSM5329 (C/A), COSM308347 (C/-), COSM5219 (C/G), COSM5152 (C/T) ; HGMD-PUBLIC CM094223, CM971273

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5152, 10473, Cosmic:5219

This variation has 18 HGVS names - click the plus to show

Variation displays