Original source

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

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

Chromosome 10:89717672 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5154, 10468

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

Variation displays