Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (C)

Chromosome 19:8974328 (forward strand) | View in location tab


with COSMIC COSM3933274 (T/C), COSM3933273 (T/C)

Most severe consequence
Missense variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 1 transcript and has 3766 sample genotypes.

Variant displays