ClinVar Miner

List of variants in gene NF1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP
GRCh37/hg19 17q11.2(chr17:29441880-29498224)x3
GRCh37/hg19 17q11.2(chr17:29479196-29562294)x3
GRCh37/hg19 17q11.2(chr17:29483858-29498224)x3
GRCh37/hg19 17q11.2(chr17:29507565-29569315)x3
GRCh37/hg19 17q11.2(chr17:29508170-29534686)x3
GRCh37/hg19 17q11.2(chr17:29516113-29534686)x3
GRCh37/hg19 17q11.2(chr17:29516113-29562294)x3
GRCh37/hg19 17q11.2(chr17:29516113-29564145)x3
GRCh37/hg19 17q11.2(chr17:29521787-29534686)x3
GRCh37/hg19 17q11.2(chr17:29521787-29536323)x3
GRCh37/hg19 17q11.2(chr17:29521833-29531143)x3
GRCh37/hg19 17q11.2(chr17:29523306-29532659)x3
GRCh37/hg19 17q11.2(chr17:29523306-29532904)x3
GRCh37/hg19 17q11.2(chr17:29523306-29534686)x3
GRCh37/hg19 17q11.2(chr17:29523306-29541844)x3
GRCh37/hg19 17q11.2(chr17:29573263-29589360)x3
GRCh37/hg19 17q11.2(chr17:29573263-29589502)x3
GRCh37/hg19 17q11.2(chr17:29573369-29589502)x3
GRCh37/hg19 17q11.2(chr17:29574712-29589502)x3
GRCh37/hg19 17q11.2(chr17:29584195-29589381)x3
GRCh37/hg19 17q11.2(chr17:29584882-29589381)x3
GRCh37/hg19 17q11.2(chr17:29654138-29700112)x3
GRCh37/hg19 17q11.2(chr17:29654876-29700112)x3
GRCh37/hg19 17q11.2(chr17:29655304-29699649)x3
GRCh37/hg19 17q11.2(chr17:29661340-29699860)x3
NM_000267.3(NF1):c.1260+1847A>C
NM_000267.3(NF1):c.1260+1859C>T
NM_000267.3(NF1):c.1260+59G>A
NM_000267.3(NF1):c.1393-130A>T
NM_000267.3(NF1):c.1393-32T>C rs2905876
NM_000267.3(NF1):c.1393-339A>G
NM_000267.3(NF1):c.1393-408T>C
NM_000267.3(NF1):c.1527+1126G>T
NM_000267.3(NF1):c.1527+1314T>A
NM_000267.3(NF1):c.1641+39T>C rs2905880
NM_000267.3(NF1):c.168C>T (p.Ser56=) rs17881168
NM_000267.3(NF1):c.1722-321G>A
NM_000267.3(NF1):c.1810T>C (p.Leu604=) rs142712751
NM_000267.3(NF1):c.1845+13A>T rs17885739
NM_000267.3(NF1):c.1933A>G (p.Met645Val) rs146051850
NM_000267.3(NF1):c.2001+198G>A
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.2544G>A (p.Gly848=) rs17883704
NM_000267.3(NF1):c.2851-16T>C rs17880825
NM_000267.3(NF1):c.288+41G>A rs2952976
NM_000267.3(NF1):c.2985G>C (p.Leu995=) rs17881467
NM_000267.3(NF1):c.3197+139T>C
NM_000267.3(NF1):c.3198-4T>C rs587782218
NM_000267.3(NF1):c.3315-130G>C
NM_000267.3(NF1):c.3496+19T>C rs9890283
NM_000267.3(NF1):c.3498C>T (p.Gly1166=) rs2066733
NM_000267.3(NF1):c.369C>G (p.Thr123=) rs146691765
NM_000267.3(NF1):c.3867C>T (p.Phe1289=) rs138186428
NM_000267.3(NF1):c.4110+1111G>A
NM_000267.3(NF1):c.4110+2114C>T
NM_000267.3(NF1):c.4368-46G>C rs17881285
NM_000267.3(NF1):c.4772+193T>C
NM_000267.3(NF1):c.4773-307A>G
NM_000267.3(NF1):c.479+208C>T
NM_000267.3(NF1):c.480-90C>T
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+117G>A
NM_000267.3(NF1):c.5546+19T>A rs2285894
NM_000267.3(NF1):c.5750-516G>T
NM_000267.3(NF1):c.5944-179A>C
NM_000267.3(NF1):c.6085-17dup rs33925668
NM_000267.3(NF1):c.61-123G>A
NM_000267.3(NF1):c.61-300C>T
NM_000267.3(NF1):c.61-4del rs551568608
NM_000267.3(NF1):c.6330C>T (p.His2110=) rs17881788
NM_000267.3(NF1):c.6579+45T>A rs17883614
NM_000267.3(NF1):c.7000-327dup
NM_000267.3(NF1):c.702G>A (p.Leu234=) rs1801052
NM_000267.3(NF1):c.7126+37C>G rs7405740
NM_000267.3(NF1):c.7127-167T>A
NM_000267.3(NF1):c.7127-260T>G
NM_000267.3(NF1):c.7127-33TTGT[3] rs149197458
NM_000267.3(NF1):c.7127-33TTGT[5] rs149197458
NM_000267.3(NF1):c.7259-17C>T rs17884859
NM_000267.3(NF1):c.730+2T>G rs200962248
NM_000267.3(NF1):c.7395-29G>A rs964288
NM_000267.3(NF1):c.7398A>G (p.Thr2466=) rs149924365
NM_000267.3(NF1):c.7532C>T (p.Ala2511Val) rs148154172
NM_000267.3(NF1):c.7692C>T (p.Ser2564=) rs17881980
NM_000267.3(NF1):c.7907+166C>T
NM_000267.3(NF1):c.7908-19G>T rs17887156
NM_000267.3(NF1):c.7908-348A>G
NM_000267.3(NF1):c.7908-8del rs564545012
NM_000267.3(NF1):c.8050+20G>A rs55747230
NM_000267.3(NF1):c.8088G>A (p.Pro2696=) rs2285895
NM_000267.3(NF1):c.8315-215T>A
NM_000267.3(NF1):c.846G>A (p.Gln282=) rs138840528
NM_000267.3(NF1):c.888+108C>T
NM_000267.3(NF1):c.888+118G>T
NM_000267.3(NF1):c.888+263C>T

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