Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.07 (C)

Chromosome 9:449874 (forward strand) | View in location tab


with COSMIC COSM3763950 (G/C), COSM3763951 (G/C)

Most severe consequence
Evidence status


Uniprot VAR_033893

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni2.5, HumanCoreExome-12

About this variant

This variant overlaps 13 transcripts and has 1137 individual genotypes.

Variation displays