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 12:109792695 (forward strand) | View in location tab

Co-located

with COSMIC COSM1358652 (C/T) ; HGMD-PUBLIC CM091510

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13177, NM_021625.3:c.1781G>A

This variation has 17 HGVS names - click the plus to show

Variation displays