Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.32 (C)
Location

Chromosome 7:99903276 (forward strand) | View in location tab

Co-located

with COSMIC COSM3762924 (T/C), COSM3762925 (T/C)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 5 transcripts and has 3787 sample genotypes.

Variant displays