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: 0.34 (C)
Location

Chromosome 19:8955583 (forward strand) | View in location tab

Co-located

with COSMIC COSM1129649 (T/C), COSM1129651 (T/C), COSM1129650 (T/C)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

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

This variation has assays on 10 chips - click the plus to show

Variation displays