ClinVar Miner

List of variants in gene NF1 reported as likely benign by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 20
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NM_000267.3(NF1):c.8416G>A (p.Ala2806Thr) rs199878086
NM_001042492.3(NF1):c.1450C>T (p.Leu484=) rs876657544
NM_001042492.3(NF1):c.2061A>G (p.Leu687=) rs143671377
NM_001042492.3(NF1):c.2619T>C (p.Arg873=) rs766212733
NM_001042492.3(NF1):c.3732T>A (p.Val1244=) rs756653022
NM_001042492.3(NF1):c.3867C>T (p.Phe1289=) rs138186428
NM_001042492.3(NF1):c.4362C>T (p.Leu1454=) rs864622298
NM_001042492.3(NF1):c.4577+11C>G rs190614908
NM_001042492.3(NF1):c.4724+11A>G rs368649260
NM_001042492.3(NF1):c.4752C>T (p.Phe1584=) rs876657545
NM_001042492.3(NF1):c.4944C>T (p.Thr1648=) rs759291615
NM_001042492.3(NF1):c.5229T>C (p.Ala1743=) rs876657546
NM_001042492.3(NF1):c.6171A>T (p.Ile2057=) rs140733963
NM_001042492.3(NF1):c.6366A>G (p.Thr2122=) rs876657547
NM_001042492.3(NF1):c.6375G>A (p.Leu2125=) rs773467465
NM_001042492.3(NF1):c.6732G>A (p.Leu2244=) rs876657548
NM_001042492.3(NF1):c.7531G>C (p.Val2511Leu) rs2230850
NM_001042492.3(NF1):c.7584A>G (p.Gln2528=) rs55865524
NM_001042492.3(NF1):c.8499T>C (p.Asn2833=) rs142636150
NM_001042492.3(NF1):c.861C>T (p.Asp287=) rs749949219

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