Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (T)

Chromosome 1:16987159 (forward strand) | View in location tab


with COSMIC COSM3750608 (C/T), COSM3750609 (C/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


ClinVar SCV000150364

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2508 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays