Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.45 (T)

Chromosome 6:49435569 (forward strand) | View in location tab


with COSMIC COSM4004063 (T/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 8 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, has 4002 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays