Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.35 (C)

Chromosome 5:136047300 (forward strand) | View in location tab


with COSMIC COSM4003288 (G/C)

Most severe consequence
Evidence status


This variation has 5 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 9 transcripts, has 1773 individual genotypes and is mentioned in 1 citation.

Variation displays