Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.16 (C)

Chromosome 15:74035865 (forward strand) | View in location tab


with COSMIC COSM3999598 (G/C) ; HGMD-PUBLIC CM097806

Most severe consequence
Missense variant
Evidence status

This variant has 18 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 20 transcripts and has 2845 sample genotypes.

Variant displays