Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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


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

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_056612

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 1 transcript and has 2759 sample genotypes.

Variant displays