Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.39 (G)

Chromosome 5:136052974 (forward strand) | View in location tab


with COSMIC COSM4159427 (A/G)

Most severe consequence
Synonymous variant
Evidence status

This variant has 8 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2535 sample genotypes and is mentioned in 2 citations.

Variant displays