Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.10 (C)
Location

Chromosome 9:449874 (forward strand) | View in location tab

Co-located

with COSMIC COSM3763951 (G/C), COSM3763950 (G/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_033893

This variant has 13 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 13 transcripts, has 2549 sample genotypes and is associated with 2 phenotypes.

Variant displays