Variants studied for Epstein-Barr virus-related tumor

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	risk factor	total
23	2	11	7	3	1	47

Gene and significance breakdown #

Total genes and gene combinations: 12

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
TP53	16	2	6	5	2	0	31
MYC	4	0	1	0	0	0	5
MST1R	0	0	0	1	0	1	2
BRCA1	0	0	1	0	0	0	1
CHEK2	1	0	0	0	0	0	1
FGFR3	0	0	1	0	0	0	1
FGFR4	0	0	0	1	0	0	1
KLHDC8B	1	0	0	0	0	0	1
KRAS	0	0	1	0	0	0	1
MET	0	0	1	0	0	0	1
NPC1	0	0	0	0	1	0	1
PMS2	1	0	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
Fulgent Genetics, Fulgent Genetics	13	2	6	6	2	0	29
OMIM	6	0	0	0	0	1	7
Pathology Department, Puerta del Mar University Hospital	0	0	4	1	0	0	5
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	0	0	1	0	1
Genome Sciences Centre, British Columbia Cancer Agency	1	0	0	0	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	1	0	0	0	0	0	1
Pele Pequeno Principe Research Institute, Faculdades Pequeno Principe	0	0	1	0	0	0	1
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	1	0	0	0	0	0	1
University Health Network, Princess Margaret Cancer Centre	1	0	0	0	0	0	1

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