Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (T)

Chromosome 11:6390705 (forward strand) | View in location tab


with COSMIC COSM1561696 (T/C), COSM1561695 (T/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ExomeChip

About this variant

This variant overlaps 27 transcripts, 1 regulatory feature, has 2538 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays