Original source

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

Alleles
A/C | Ambiguity code: M
Location

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

Co-located

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74286221

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

Genotyping chips

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

About this variant

This variant overlaps 22 transcripts and has 1 individual genotype.

Variation displays