Original source

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

A/C | Ambiguity code: M

Chromosome 3:184380405 (forward strand) | View in location tab


with COSMIC COSM4157476 (A/C), COSM4157477 (A/C)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs74286221

This variant has 11 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 21 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays