Original source

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

A/G | Ancestral: A | Ambiguity code: R | 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

This variant has 9 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2588 sample genotypes and is associated with 1 phenotype.

Variant displays