Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.31 (G)
Location

Chromosome 16:3249749 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754868 (G/A), COSM3754869 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 16 transcripts, has 2925 individual genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variation displays