Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.24 (C)

Chromosome 9:712060 (forward strand) | View in location tab


with COSMIC COSM1132467 (G/C), COSM1132465 (G/C)

Most severe consequence
Missense variant
Evidence status


This variant has 4 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts and has 2990 sample genotypes.

Variant displays