Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (T)

Chromosome 4:54100752 (forward strand) | View in location tab


with COSMIC COSM1328491 (T/C)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs2278140, rs3194385

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays