Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.08 (T)

Chromosome 10:69401072 (forward strand) | View in location tab


with COSMIC COSM4144807 (C/T), COSM4144809 (C/T), COSM4144808 (C/T), COSM4144810 (C/T)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs3750791

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts and has 3730 sample genotypes.

Variant displays