Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.15 (A)

Chromosome 11:6394233 (forward strand) | View in location tab


with COSMIC COSM3752609 (G/A), COSM3752608 (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 7 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 27 transcripts, has 4084 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays