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 | MAF: < 0.01 (T)
Location

Chromosome 12:109792396 (forward strand) | View in location tab

Co-located

with COSMIC COSM96812 (C/T) ; HGMD-PUBLIC CM083203

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13176

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

Variation displays