Original source

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

C/G/T | Ancestral: C | Ambiguity code: B | MAF: 0.08 (G)

Chromosome 1:186679065 (forward strand) | View in location tab


with COSMIC COSM146712 (C/G)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 12 transcripts, has 3781 sample genotypes and is mentioned in 28 citations.

Variant displays