Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.39 (G)
Location

Chromosome 16:3254762 (forward strand) | View in location tab

Co-located

with COSMIC COSM435205 (A/G)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

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

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 3771 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays