Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.10 (G)

Chromosome 4:3518035 (forward strand) | View in location tab


with COSMIC COSM4159037 (A/G)

Most severe consequence
Splice region variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts and has 2537 sample genotypes.

Variant displays