Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.23 (C)

Chromosome 5:161854239 (forward strand) | View in location tab


with COSMIC COSM4003435 (T/C)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3690 sample genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variant displays