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 10:101770378 (forward strand) | View in location tab

Co-located

with COSMIC COSM1345400 (G/A) ; HGMD-PUBLIC CM082674

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9234

This variation has 13 HGVS names - click the plus to show

Variation displays