Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)

Chromosome 14:20472467 (forward strand) | View in location tab


with COSMIC COSM147734 (C/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 9 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4113 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays