Variants studied for adrenocortical carcinoma, hereditary

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
55	36	76	5	2	172

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
TP53	55	36	76	5	2	172

Submitter and significance breakdown #

Total submitters: 6

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Baylor Genetics	46	33	72	0	0	151
Fulgent Genetics, Fulgent Genetics	13	2	6	5	2	28
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	3	0	1	0	0	4
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	0	1	0	0	0	1
Genome-Nilou Lab	1	0	0	0	0	1
Suma Genomics	1	0	0	0	0	1

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