Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.38 (A)

Chromosome 7:10982603 (forward strand) | View in location tab


with COSMIC COSM3723030 (A/G), COSM3723031 (A/G)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_Human660W-quad, HumanCoreExome-12

About this variant

This variant overlaps 5 transcripts and has 2293 individual genotypes.

Variation displays