ClinVar Miner

List of variants in gene NF1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

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Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP
NM_000267.3(NF1):c.1186-13delT rs763903212
NM_000267.3(NF1):c.1393-32T>C rs2905876
NM_000267.3(NF1):c.1641+39T>C rs2905880
NM_000267.3(NF1):c.168C>T (p.Ser56=) rs17881168
NM_000267.3(NF1):c.1810T>C (p.Leu604=) rs142712751
NM_000267.3(NF1):c.1845+13A>T rs17885739
NM_000267.3(NF1):c.1846-12A>T rs188510882
NM_000267.3(NF1):c.1846-39C>T rs17885830
NM_000267.3(NF1):c.1933A>G (p.Met645Val) rs146051850
NM_000267.3(NF1):c.2022C>T (p.Ser674=) rs2230851
NM_000267.3(NF1):c.2034G>A (p.Pro678=) rs2285892
NM_000267.3(NF1):c.2252-31A>T rs141082540
NM_000267.3(NF1):c.2252-34T>C rs200937398
NM_000267.3(NF1):c.2544G>A (p.Gly848=) rs17883704
NM_000267.3(NF1):c.2851-16T>C rs17880825
NM_000267.3(NF1):c.2985G>C (p.Leu995=) rs17881467
NM_000267.3(NF1):c.3496+33C>A rs2066736
NM_000267.3(NF1):c.3498C>T (p.Gly1166=) rs2066733
NM_000267.3(NF1):c.3974+38T>G rs9894862
NM_000267.3(NF1):c.3974+9T>A rs368586596
NM_000267.3(NF1):c.4515-39A>G rs8072417
NM_000267.3(NF1):c.4772+36T>C rs16972128
NM_000267.3(NF1):c.4819T>C (p.Leu1607=) rs10512435
NM_000267.3(NF1):c.4866G>A (p.Val1622=) rs17880521
NM_000267.3(NF1):c.4972A>G (p.Ile1658Val) rs147327414
NM_000267.3(NF1):c.5172G>A (p.Lys1724=) rs17887014
NM_000267.3(NF1):c.5205+23T>C rs9894648
NM_000267.3(NF1):c.528T>A (p.Asp176Glu) rs112306990
NM_000267.3(NF1):c.5546+19T>A rs2285894
NM_000267.3(NF1):c.6085-29delT rs398100472
NM_000267.3(NF1):c.61-14delT rs376172637
NM_000267.3(NF1):c.61-4delT rs551568608
NM_000267.3(NF1):c.6330C>T (p.His2110=) rs17881788
NM_000267.3(NF1):c.702G>A (p.Leu234=) rs1801052
NM_000267.3(NF1):c.7126+37C>G rs7405740
NM_000267.3(NF1):c.7127-33TTGT[3] rs149197458
NM_000267.3(NF1):c.7259-17C>T rs17884859
NM_000267.3(NF1):c.730+32delT rs71142032
NM_000267.3(NF1):c.7395-29G>A rs964288
NM_000267.3(NF1):c.7398A>G (p.Thr2466=) rs149924365
NM_000267.3(NF1):c.7552+24delA rs754290122
NM_000267.3(NF1):c.7692C>T (p.Ser2564=) rs17881980
NM_000267.3(NF1):c.7908-19G>T rs17887156
NM_000267.3(NF1):c.7908-8delT rs564545012
NM_000267.3(NF1):c.8050+20G>A rs55747230
NM_000267.3(NF1):c.8098-34delA rs528599051
NM_000267.3(NF1):c.846G>A (p.Gln282=) rs138840528
NM_001042492.2(NF1):c.889-25_889-21delTTATC rs17881173

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