Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

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

Co-located

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

About this variant

This variant overlaps 1 transcript and has 2759 individual genotypes.

Variation displays