Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.36 (G)

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


with COSMIC COSM4159427 (A/G)

Most severe consequence
Evidence status

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

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

About this variant

This variant overlaps 11 transcripts, has 1492 individual genotypes and is mentioned in 2 citations.

Variation displays