ClinVar Miner

Variants studied for adult glioblastoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign other not provided total
1 223 0 0 0 3 2 229

Gene and significance breakdown #

Total genes and gene combinations: 22
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Gene or gene combination pathogenic likely pathogenic other not provided total
TP53 0 120 0 0 120
PIK3CA 0 45 0 0 45
EGFR 0 11 0 0 11
MTOR 0 7 0 0 7
PTEN 0 5 0 1 6
BRAF 0 5 0 0 5
FBXW7 0 5 0 0 5
IDH1 0 5 0 0 5
NRAS 0 5 0 0 5
CREBBP 0 4 0 0 4
HRAS, LRRC56 0 3 0 0 3
FGFR1 0 2 0 0 2
H3F3A 0 1 1 0 2
ATM, C11orf65 0 1 0 0 1
BCOR 0 0 1 0 1
DNMT3A 0 1 0 0 1
MED12 0 0 1 0 1
MGMT 0 0 0 1 1
MSH2 1 0 0 0 1
MYCN, MYCNOS 0 1 0 0 1
PIK3R1 0 1 0 0 1
POLE 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic other not provided total
Database of Curated Mutations (DoCM) 0 221 0 2 223
Donald Williams Parsons Laboratory,Baylor College of Medicine 0 0 3 0 3
Clinical Genomics Lab,St. Jude Children's Research Hospital 1 1 0 0 2
Murat Gunel Laboratory,Yale University 0 1 0 0 1

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