Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (C)

Chromosome 16:28887472 (forward strand) | View in location tab


with COSMIC COSM3754834 (T/C)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 8 transcripts, has 3728 sample genotypes and is associated with 2 phenotypes.

Variant displays