ClinVar Miner

List of variants in gene DICER1 reported as likely benign for childhood malignant neoplasm

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_177438.3(DICER1):c.1377-4T>G rs192490028 0.00240
NM_177438.3(DICER1):c.4891T>G (p.Ser1631Ala) rs145551486 0.00128
NM_177438.3(DICER1):c.1908-4A>G rs112284114 0.00123
NM_177438.3(DICER1):c.3213A>G (p.Arg1071=) rs148959399 0.00123
NM_177438.3(DICER1):c.5604-12G>A rs149841885 0.00122
NM_177438.3(DICER1):c.*2359_*2360del rs200215778 0.00115
NM_177438.3(DICER1):c.*1894C>T rs540809100 0.00041
NM_177438.3(DICER1):c.3269+14G>A rs201906274 0.00040
NM_177438.3(DICER1):c.1329C>T (p.Cys443=) rs776143079 0.00004
NM_177438.3(DICER1):c.4899A>G (p.Val1633=) rs878855271 0.00003
NM_177438.3(DICER1):c.4796G>A (p.Arg1599Gln) rs569615549 0.00002
NM_177438.3(DICER1):c.1770T>C (p.Cys590=) rs777355058 0.00001
NM_177438.3(DICER1):c.2553G>A (p.Gln851=) rs373715574 0.00001
NM_177438.3(DICER1):c.2718C>T (p.Arg906=) rs370692165 0.00001
NM_177438.3(DICER1):c.3269+12C>T rs775380766 0.00001
NM_177438.3(DICER1):c.*2751GAT[1] rs573135025
NM_177438.3(DICER1):c.1510-4del rs546524688
NM_177438.3(DICER1):c.1510-4dup rs546524688
NM_177438.3(DICER1):c.2613C>T (p.Asp871=) rs759827733
NM_177438.3(DICER1):c.4254GGA[2] (p.Glu1420del) rs544960260
NM_177438.3(DICER1):c.4608T>C (p.Gly1536=) rs1890331241
NM_177438.3(DICER1):c.4807C>T (p.Leu1603=) rs201320420

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