ClinVar Miner

Variants studied for chronic myelogenous leukemia, BCR-ABL1 positive

Included ClinVar conditions (2):
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 not provided total
0 31 0 0 0 7 38

Gene and significance breakdown #

Total genes and gene combinations: 10
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Gene or gene combination likely pathogenic not provided total
ABL1 26 1 27
BCR 0 2 2
CSF3R 2 0 2
BCR, LOC107963955 0 1 1
BRAF 1 0 1
FLT3, MYO18A 1 0 1
INSL6, JAK2 0 1 1
KIT 0 1 1
NRAS 1 0 1
SETBP1 0 1 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter likely pathogenic not provided total
Database of Curated Mutations (DoCM) 30 4 34
Laboratory of Molecular Diagnostics and Monitoring of CML and Ph+ Leukemias, Institute of Hematology and Blood Transfusion 0 3 3
Knight Cancer Institute,Oregon Health and Science University 1 0 1

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