Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.29 (C)

Chromosome 5:150115832 (forward strand) | View in location tab


with COSMIC COSM149993 (T/C)

Most severe consequence
Evidence status


Archive dbSNP rs58690245

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 1405 individual genotypes and is mentioned in 1 citation.

Variation displays