ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 140
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HGVS dbSNP
NM_000267.3(NF1):c.1032A>G (p.Leu344=) rs199832006
NM_000267.3(NF1):c.1063-122T>G
NM_000267.3(NF1):c.1063-205G>A
NM_000267.3(NF1):c.1137C>T (p.Cys379=) rs139648455
NM_000267.3(NF1):c.1176A>G (p.Gln392=) rs566220983
NM_000267.3(NF1):c.1186-8T>C
NM_000267.3(NF1):c.1260+1334T>C
NM_000267.3(NF1):c.1393-20T>C rs1057523234
NM_000267.3(NF1):c.1429T>C (p.Phe477Leu) rs1555612276
NM_000267.3(NF1):c.1527+1465G>T
NM_000267.3(NF1):c.1527+238C>T
NM_000267.3(NF1):c.1527+241A>G
NM_000267.3(NF1):c.153T>C (p.Phe51=) rs1057523892
NM_000267.3(NF1):c.1545G>T (p.Gly515=) rs876658203
NM_000267.3(NF1):c.1548C>G (p.Pro516=) rs768883989
NM_000267.3(NF1):c.1588G>A (p.Val530Ile) rs145191978
NM_000267.3(NF1):c.1642-158A>G
NM_000267.3(NF1):c.1642-659T>C
NM_000267.3(NF1):c.1650G>C (p.Leu550=) rs1555613190
NM_000267.3(NF1):c.1728A>G (p.Gln576=) rs1057523206
NM_000267.3(NF1):c.1734T>C (p.Leu578=) rs876658128
NM_000267.3(NF1):c.1810T>C (p.Leu604=) rs142712751
NM_000267.3(NF1):c.1845+14C>T rs1057523395
NM_000267.3(NF1):c.1846-12A>T rs188510882
NM_000267.3(NF1):c.1846-178A>C
NM_000267.3(NF1):c.1994C>T (p.Ser665Phe) rs145891889
NM_000267.3(NF1):c.2002-9G>T rs376197466
NM_000267.3(NF1):c.2061A>G (p.Leu687=) rs143671377
NM_000267.3(NF1):c.2133C>T (p.Arg711=) rs148085908
NM_000267.3(NF1):c.2142T>C (p.Cys714=) rs141382637
NM_000267.3(NF1):c.2160G>T (p.Arg720=) rs765339408
NM_000267.3(NF1):c.2178G>C (p.Val726=) rs369590240
NM_000267.3(NF1):c.2238T>C (p.Asn746=) rs768161162
NM_000267.3(NF1):c.2251+203G>T
NM_000267.3(NF1):c.2252-34T>C rs200937398
NM_000267.3(NF1):c.2294G>A (p.Arg765His) rs199474777
NM_000267.3(NF1):c.237A>G (p.Leu79=) rs752208826
NM_000267.3(NF1):c.2410-13A>T rs1567848711
NM_000267.3(NF1):c.2490C>T (p.Asp830=) rs786201629
NM_000267.3(NF1):c.2514C>T (p.Ile838=) rs863224352
NM_000267.3(NF1):c.2547A>C (p.Gly849=) rs748303121
NM_000267.3(NF1):c.2553C>T (p.Cys851=) rs2230852
NM_000267.3(NF1):c.2640G>A (p.Val880=) rs786202443
NM_000267.3(NF1):c.2838C>T (p.Asp946=) rs147188807
NM_000267.3(NF1):c.2889A>G (p.Gln963=) rs1567849526
NM_000267.3(NF1):c.289-12T>C rs1486449114
NM_000267.3(NF1):c.289-1886A>G
NM_000267.3(NF1):c.2985G>C (p.Leu995=) rs17881467
NM_000267.3(NF1):c.2991-6A>G rs1191095886
NM_000267.3(NF1):c.2991-97T>C
NM_000267.3(NF1):c.3045G>A (p.Leu1015=) rs926335233
NM_000267.3(NF1):c.3063A>C (p.Val1021=) rs768611775
NM_000267.3(NF1):c.3197+505C>T
NM_000267.3(NF1):c.3197+9dup rs755212937
NM_000267.3(NF1):c.3198-289A>G
NM_000267.3(NF1):c.3315-8T>C rs764783865
NM_000267.3(NF1):c.340C>T (p.Leu114=) rs7207410
NM_000267.3(NF1):c.3468C>T (p.Asn1156=) rs147955381
NM_000267.3(NF1):c.3690G>A (p.Val1230=) rs183296277
NM_000267.3(NF1):c.3709-8G>C rs767650263
NM_000267.3(NF1):c.3867C>T (p.Phe1289=) rs138186428
NM_000267.3(NF1):c.3871-15C>T
NM_000267.3(NF1):c.3871-4G>C rs558421445
NM_000267.3(NF1):c.3883A>G (p.Thr1295Ala) rs143836226
NM_000267.3(NF1):c.3916C>A (p.Arg1306=) rs376576925
NM_000267.3(NF1):c.3974+528C>A
NM_000267.3(NF1):c.4110+15dup rs763846160
NM_000267.3(NF1):c.4111-264T>C
NM_000267.3(NF1):c.4111-287G>A
NM_000267.3(NF1):c.4111-8_4111-6del rs751729752
NM_000267.3(NF1):c.4143C>T (p.Ile1381=) rs864622406
NM_000267.3(NF1):c.4206A>G (p.Glu1402=) rs17886566
NM_000267.3(NF1):c.4367+72C>T
NM_000267.3(NF1):c.4514+11C>G rs190614908
NM_000267.3(NF1):c.4514+12C>T rs17878332
NM_000267.3(NF1):c.4563T>C (p.Leu1521=) rs1555619012
NM_000267.3(NF1):c.456A>C (p.Ala152=) rs377481833
NM_000267.3(NF1):c.4661+11A>G rs368649260
NM_000267.3(NF1):c.4686A>G (p.Glu1562=) rs144091165
NM_000267.3(NF1):c.4772+36T>C rs16972128
NM_000267.3(NF1):c.4773-11A>G rs1437937029
NM_000267.3(NF1):c.479+4A>G rs1567818032
NM_000267.3(NF1):c.4881C>T (p.Thr1627=) rs759291615
NM_000267.3(NF1):c.4986C>T (p.Asn1662=) rs140994965
NM_000267.3(NF1):c.5172G>A (p.Lys1724=) rs17887014
NM_000267.3(NF1):c.5205+157A>T
NM_000267.3(NF1):c.5206-265T>C
NM_000267.3(NF1):c.5217T>C (p.Thr1739=) rs779104728
NM_000267.3(NF1):c.5694G>A (p.Glu1898=) rs141077224
NM_000267.3(NF1):c.5749+110T>G
NM_000267.3(NF1):c.5750-14G>A rs779945790
NM_000267.3(NF1):c.5750-5dup rs775451791
NM_000267.3(NF1):c.586+251A>G
NM_000267.3(NF1):c.586+273A>G
NM_000267.3(NF1):c.5895A>G (p.Lys1965=) rs1216926117
NM_000267.3(NF1):c.5944-286A>G
NM_000267.3(NF1):c.5970A>G (p.Leu1990=) rs147995863
NM_000267.3(NF1):c.60+217C>T
NM_000267.3(NF1):c.6084+8C>G rs182709912
NM_000267.3(NF1):c.6108A>T (p.Ile2036=) rs140733963
NM_000267.3(NF1):c.6522G>A (p.Glu2174=) rs202151774
NM_000267.3(NF1):c.6561T>C (p.Ala2187=) rs746061888
NM_000267.3(NF1):c.6641+3A>G rs375560135
NM_000267.3(NF1):c.6771C>T (p.Cys2257=) rs149603406
NM_000267.3(NF1):c.6816T>C (p.Ala2272=) rs761125983
NM_000267.3(NF1):c.681T>C (p.Tyr227=) rs745804540
NM_000267.3(NF1):c.6858+117A>G
NM_000267.3(NF1):c.6859-14_6859-13del rs146785663
NM_000267.3(NF1):c.7127-33TTGT[4] rs149197458
NM_000267.3(NF1):c.7127-33TTGT[7] rs149197458
NM_000267.3(NF1):c.7258+13A>G rs1057523308
NM_000267.3(NF1):c.7258+19_7258+22del rs528866152
NM_000267.3(NF1):c.7259-16A>G rs369168102
NM_000267.3(NF1):c.7260T>G (p.Ala2420=) rs765750009
NM_000267.3(NF1):c.7269A>G (p.Thr2423=) rs759005886
NM_000267.3(NF1):c.730+16dup rs373999174
NM_000267.3(NF1):c.731-114A>G
NM_000267.3(NF1):c.731-6A>C rs369366499
NM_000267.3(NF1):c.7394+21A>G
NM_000267.3(NF1):c.7394+8G>T rs376147282
NM_000267.3(NF1):c.7395-7C>T rs758106590
NM_000267.3(NF1):c.7398A>G (p.Thr2466=) rs149924365
NM_000267.3(NF1):c.7468G>C (p.Val2490Leu) rs2230850
NM_000267.3(NF1):c.7521A>G (p.Gln2507=) rs55865524
NM_000267.3(NF1):c.7552+271C>T
NM_000267.3(NF1):c.7675+46G>A rs199641099
NM_000267.3(NF1):c.7807-13dup rs369360556
NM_000267.3(NF1):c.7847G>A (p.Arg2616Gln) rs560262404
NM_000267.3(NF1):c.7908-8del rs564545012
NM_000267.3(NF1):c.7923C>T (p.Asp2641=) rs876658550
NM_000267.3(NF1):c.7978A>G (p.Ile2660Val) rs146315101
NM_000267.3(NF1):c.8050+22del rs563852879
NM_000267.3(NF1):c.8088G>A (p.Pro2696=) rs2285895
NM_000267.3(NF1):c.8331C>T (p.Asn2777=) rs376136174
NM_000267.3(NF1):c.8332G>A (p.Val2778Ile) rs377393842
NM_000267.3(NF1):c.8388C>T (p.Ser2796=) rs547090599
NM_000267.3(NF1):c.8436T>C (p.Asn2812=) rs142636150
NM_000267.3(NF1):c.846G>A (p.Gln282=) rs138840528
NM_000267.3(NF1):c.861C>T (p.Asp287=) rs749949219
NM_000267.3(NF1):c.889-192G>T

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