Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.23 (A)

Chromosome 16:55697923 (forward strand) | View in location tab


with COSMIC COSM3754933 (G/A), COSM3754932 (G/A)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 30 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 18 transcripts, has 3748 sample genotypes and is mentioned in 21 citations.

Variant displays