Original source

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

C/G | Ancestral: G | Ambiguity code: S | MAF: 0.37 (C)

Chromosome 7:87935182 (forward strand) | View in location tab


with COSMIC COSM3750054 (C/G), COSM3750053 (C/G), COSM3750055 (C/G)

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 8 transcripts, has 1479 individual genotypes and is mentioned in 3 citations.

Variation displays