Original source

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

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

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


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

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4066 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays