Original source

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

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.17 (C)

Chromosome 8:127416411 (forward strand) | View in location tab


with COSMIC COSM3982389 (A/G), COSM3834039 (A/C), COSM3834038 (A/C), COSM3982388 (A/G)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts and has 1097 individual genotypes.

Variation displays