Original source

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

Alleles
C/T | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 19:8959510 (forward strand) | View in location tab

Co-located

with COSMIC COSM3423412 (C/T), COSM3423414 (C/T), COSM3423413 (C/T)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_056612

This variation has 3 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays