Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.06 (G)
Location

Chromosome 16:47697618 (forward strand) | View in location tab

Co-located

with COSMIC COSM1629903 (A/T), COSM1629904 (A/T), COSM1629902 (A/T) ; HGMD-PUBLIC CM031328

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays