Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (C)

Chromosome 9:121332522 (forward strand) | View in location tab


with COSMIC COSM1459763 (T/C), COSM1459764 (T/C)

Most severe consequence
Evidence status


Archive dbSNP rs3191330, rs1050966

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and has 1284 individual genotypes.

Variation displays