Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 10:16890385 (forward strand) | View in location tab

Co-located

with COSMIC COSM32707 (G/A)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_035831

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2505 individual genotypes and is associated with 1 phenotype.

Variation displays