Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.32 (G)
Location

Chromosome 5:135028828 (forward strand) | View in location tab

Co-located

with COSMIC COSM3760918 (C/G)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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 10 transcripts, has 2534 individual genotypes and is mentioned in 2 citations.

Variation displays