Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.45 (A)

Chromosome 1:16992516 (forward strand) | View in location tab


with COSMIC COSM3997075 (G/A), COSM3997076 (G/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 24 transcripts, has 2549 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays