Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 5:254484 (forward strand) | View in location tab

Co-located

with COSMIC COSM1666612 (A/T) ; dbSNP rs34482117 (A/T)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 19 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays