ClinVar Miner

Variants studied for adrenal cortex neoplasm

Included ClinVar conditions (7):
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 total
23 67 6 0 0 95

Gene and significance breakdown #

Total genes and gene combinations: 12
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
TP53 5 40 4 48
CLCN2 11 0 1 12
CTNNB1 0 11 0 11
NRAS 0 5 0 5
PIK3CA 0 4 0 4
ATP1A1 3 0 0 3
ATP2B3 3 0 0 3
BRAF 0 3 0 3
GNAS 0 3 0 3
CHEK2 0 0 1 1
H3F3A 0 1 0 1
MEN1 1 0 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance total
Database of Curated Mutations (DoCM) 0 65 0 65
Fulgent Genetics 5 1 5 11
OMIM 7 0 0 7
Institute of Human Genetics,Klinikum rechts der Isar 7 0 0 7
Ute Scholl Laboratory,Heinrich Heine University Duesseldorf 5 0 0 5
Donald Williams Parsons Laboratory,Baylor College of Medicine 0 1 0 1
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 1 1

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