Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.32 (C)
Location

Chromosome 14:102514227 (forward strand) | View in location tab

Co-located

with COSMIC COSM147844 (T/C)

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays