HAS_CLnhV

Annotation_Transcript - Transcript annotation

COSMIChsCnt - number of samples in COSMIC with this mutation

Codon_Change - Codon change due to genetic variant.

ExAC_AF - the allelic frequency in the Exome Aggregation Consortium (ExAC)

Genome_Change - Genome position change due to genetic variant.

HC_AC - in Broad Hybrid capture data from the CCLE2 project

Protein_Change - Protein (amino acid/position) change due to genetic variant.

RD_AC - in Broad Raindance data from the CCLE2 project

RNAseq_AC - in Broad RNAseq data from the CCLE2 project

Reference_Allele - Reference allele

SangerRecalibWES_AC - in Sanger WES after realignment at Broad

SangerWES_AC - in Sanger WES

TCGAhsCnt - number of times this mutation is observed in TCGA

Tumor_Seq_Allele1 - Variant allele

WES_AC - CCLE WES data from the CCLE2 project

WGS_AC - in Broad WGS data from the CCLE2 project

cDNA_Change - cDNA change due to genetic variant.

isCOSMIChotspot - is this mutation commonly found in COSMIC

isDeleterious - True/False if variant is deleterious

isTCGAhotspot - is this mutation commonly found in TCGA

sources - Cancer Cell Line Encyclopedia

variant_classification - Variant classification (e.g. Missense_Mutation, Frame_Shift_Del, Silent, etc.)

variant_type - SNP, DEL, INS, DNP, or TNP

all properties with AC, the allelic ratio is presented as [ALTERNATE:REFERENCE].