Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.39 (C)
Location

Chromosome 16:3254654 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754870 (T/C)

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

About this variant

This variant overlaps 15 transcripts, has 2567 sample genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variant displays