Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.30 (G)
Location

Chromosome 12:12718165 (forward strand) | View in location tab

Co-located

with COSMIC COSM4146812 (T/G) ; HGMD-PUBLIC CM033961

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

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

This variation has assays on 10 chips - click the plus to show

Variation displays