Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (C)
Location

Chromosome 15:71812093 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754454 (T/C), COSM3754456 (T/C), COSM3754455 (T/C)

Most severe consequence
Evidence status

This variation has 2 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

Variation displays