Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.42 (G)

Chromosome 11:17498195 (forward strand) | View in location tab


with COSMIC COSM3736035 (C/G), COSM3736036 (C/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 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 9 transcripts, 1 regulatory feature, has 3156 sample genotypes and is associated with 1 phenotype.

Variant displays