Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 6 synonyms - click the plus to show

This variant has 13 HGVS names - click the plus to 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