Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/A/C | Ancestral: C | Ambiguity code: H | MAF: 0.39 (C)

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


with COSMIC COSM3754870 (T/C)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 46 HGVS names - Show

About this variant

This variant overlaps 30 transcripts, has 2567 sample genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variant displays