Whole-Genome and Exome Sequencing in Clear-Cell Renal Cell Carcinoma
Anthropometry (1)
- BMI - Body Mass Index (phv00168013.v1.p1)
Demographics (2)
- Age - Disease onset age (phv00168011.v1.p1)
- Sex - Gender of participant (phv00168012.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Case control status of the subject (phv00168007.v1.p1)
Race and Ethnicity (1)
- Race - Race of participant (phv00168014.v1.p1)
Other (25)
- ANALYTE_TYPE - Analyte Type (phv00168024.v1.p1)
- BAP1 - Somatic mutation in BAP1 (Entrez GeneID: 8314) (phv00168019.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00168023.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00168006.v1.p1)
- Disease - Disease of the patient (phv00168015.v1.p1)
- GEO_ACCESSION - GEO accession ID (phv00168098.v1.p1)
- Grade - Fuhrman grade (phv00168018.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00168026.v1.p1)
- IS_TUMOR - Tumor status (phv00168025.v1.p1)
- PBRM1 - Somatic mutation in PBRM1 (Entrez GeneID: 55193) (phv00168020.v1.p1)
- PRIMARY_METASTATIC_TUMOR - Primary tumor, metastasis, or transformed cell line (phv00168027.v1.p1)
- PRIMARY_TUMOR_LOCATION - Primary tumor location (phv00168028.v1.p1)
- SAMPID - De-identified Sample ID (phv00168022.v1.p1)
- SAMPID - Sample ID (phv00168009.v1.p1)
- SAMPID - Sample ID (phv00168097.v1.p1)
- SAMPLE_USE - Sample Use. SNP_Array: SNP genotypes obtained using standard or custom microarrays; WES_SRA: Whole exome sequencing data available through SRA; WGS_SRA: Whole genome sequencing data available through SRA; totRNA_Expression: Expression data for total RNA sample (array data) (phv00168096.v1.p1)
- Stage - Stage (phv00168017.v1.p1)
- SUBJID - De-identified Subject ID (phv00168010.v1.p1)
- SUBJID - Subject ID (phv00168005.v1.p1)
- SUBJID - Subject ID (phv00168008.v1.p1)
- TNM - TNM staging (phv00168016.v1.p1)
- TUMOR_GRADE - Tumor grade of sample (phv00168030.v1.p1)
- TUMOR_STAGE - Tumor stage of sample (phv00168029.v1.p1)
- TUMOR_TREATMENT - Type of tumor treatment for sample (phv00168031.v1.p1)
- VHL - Somatic mutation in VHL (Entrez GeneID: 7428) (phv00168021.v1.p1)