Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.35 (G)

Chromosome 4:6302228 (forward strand) | View in location tab


with COSMIC COSM3760688 (G/A) ; HGMD-PUBLIC CM021365

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 4 HGVS names - click the plus to show

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 4066 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays