Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.35 (C)

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


with COSMIC COSM1129650 (T/C), COSM1129651 (T/C), COSM1129649 (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 3765 sample genotypes.

Variant displays