Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (A)
Location

Chromosome 9:127912633 (forward strand) | View in location tab

Co-located

with COSMIC COSM3685503 (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 12 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and has 3240 sample genotypes.

Variant displays