Original source

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

A/G/T | Ancestral: A | Ambiguity code: D | MAF: 0.24 (A)

Chromosome 11:71435645 (forward strand) | View in location tab


with COSMIC COSM1475860 (A/G), COSM429787 (A/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 16 transcripts, has 3912 sample genotypes and is associated with 1 phenotype.

Variant displays