Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 10:87957915 (forward strand) | View in location tab

Co-located

with COSMIC COSM33990 (C/GGGAGG), COSM69004 (C/-), COSM13457 (C/A), COSM5154 (C/T) ; HGMD-PUBLIC CM971277

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5154, 10468

This variation has 8 HGVS names - click the plus to show

Variation displays