ClinVar Miner

List of variants in gene NF1 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP
NM_000267.3(NF1):c.*1164G>A rs140110377
NM_000267.3(NF1):c.*2089G>A rs17881973
NM_000267.3(NF1):c.*2201G>A rs7406983
NM_000267.3(NF1):c.*2265C>G rs1800845
NM_000267.3(NF1):c.*2829T>C rs1048317
NM_000267.3(NF1):c.*498T>G rs9900729
NM_000267.3(NF1):c.*4T>C rs201044568
NM_000267.3(NF1):c.*871A>T rs568276164
NM_000267.3(NF1):c.*873A>T rs3058624
NM_000267.3(NF1):c.1005T>C (p.Asn335=) rs777369021
NM_000267.3(NF1):c.1032A>G (p.Leu344=) rs199832006
NM_000267.3(NF1):c.1137C>T (p.Cys379=) rs139648455
NM_000267.3(NF1):c.1599C>G (p.Val533=) rs369458366
NM_000267.3(NF1):c.1933A>G (p.Met645Val) rs146051850
NM_000267.3(NF1):c.1976G>A (p.Arg659Gln) rs151138158
NM_000267.3(NF1):c.2178G>C (p.Val726=) rs369590240
NM_000267.3(NF1):c.2211A>T (p.Thr737=) rs1178560430
NM_000267.3(NF1):c.2252-31A>T rs141082540
NM_000267.3(NF1):c.2252-34T>C rs200937398
NM_000267.3(NF1):c.2617C>T (p.Arg873Cys) rs199474739
NM_000267.3(NF1):c.2921A>G (p.Asn974Ser) rs557875547
NM_000267.3(NF1):c.3198-3dup rs1555614816
NM_000267.3(NF1):c.3198-4T>C rs587782218
NM_000267.3(NF1):c.321G>A (p.Thr107=) rs786201731
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.369C>G (p.Thr123=) rs146691765
NM_000267.3(NF1):c.4111-8_4111-6del rs751729752
NM_000267.3(NF1):c.4358C>T (p.Ala1453Val) rs587781553
NM_000267.3(NF1):c.4788A>G (p.Gln1596=) rs150309802
NM_000267.3(NF1):c.4986C>T (p.Asn1662=) rs140994965
NM_000267.3(NF1):c.5749+8A>G rs372075322
NM_000267.3(NF1):c.5820G>A (p.Lys1940=) rs144808600
NM_000267.3(NF1):c.6316A>G (p.Ile2106Val) rs200022550
NM_000267.3(NF1):c.731-6A>C rs369366499
NM_000267.3(NF1):c.7347T>C (p.Asn2449=) rs17881903
NM_000267.3(NF1):c.7470C>T (p.Val2490=) rs760733171
NM_000267.3(NF1):c.7532C>T (p.Ala2511Val) rs148154172
NM_000267.3(NF1):c.7978A>G (p.Ile2660Val) rs146315101
NM_000267.3(NF1):c.8452G>A (p.Val2818Met) rs368149035
NM_000267.3(NF1):c.960T>A (p.Ala320=) rs376447070
NM_001042492.2(NF1):c.*859_*860AT[7] rs369548314
NM_001042492.3(NF1):c.*1481A>G
NM_001042492.3(NF1):c.*2777C>T
NM_001042492.3(NF1):c.*29A>G rs139147882
NM_001042492.3(NF1):c.*3514G>A
NM_001042492.3(NF1):c.*585G>T
NM_001042492.3(NF1):c.*971T>A
NM_001042492.3(NF1):c.168C>T (p.Ser56=) rs17881168
NM_001042492.3(NF1):c.1810T>C (p.Leu604=) rs142712751
NM_001042492.3(NF1):c.1994C>T (p.Ser665Phe) rs145891889
NM_001042492.3(NF1):c.2022C>T (p.Ser674=) rs2230851
NM_001042492.3(NF1):c.2033C>T (p.Pro678Leu) rs17881753
NM_001042492.3(NF1):c.2034G>A (p.Pro678=) rs2285892
NM_001042492.3(NF1):c.2544G>A (p.Gly848=) rs17883704
NM_001042492.3(NF1):c.2553C>T (p.Cys851=) rs2230852
NM_001042492.3(NF1):c.2985G>C (p.Leu995=) rs17881467
NM_001042492.3(NF1):c.3197+9dup rs755212937
NM_001042492.3(NF1):c.3198-4dup rs371047262
NM_001042492.3(NF1):c.3270A>C (p.Gly1090=) rs150015024
NM_001042492.3(NF1):c.3498C>T (p.Gly1166=) rs2066733
NM_001042492.3(NF1):c.3867C>T (p.Phe1289=) rs138186428
NM_001042492.3(NF1):c.3974+23A>T rs376217184
NM_001042492.3(NF1):c.4269A>G (p.Glu1423=) rs17886566
NM_001042492.3(NF1):c.4578-12dup rs1597748630
NM_001042492.3(NF1):c.4882T>C (p.Leu1628=) rs10512435
NM_001042492.3(NF1):c.4929G>A (p.Val1643=) rs17880521
NM_001042492.3(NF1):c.5035A>G (p.Ile1679Val) rs147327414
NM_001042492.3(NF1):c.5235G>A (p.Lys1745=) rs17887014
NM_001042492.3(NF1):c.528T>A (p.Asp176Glu) rs112306990
NM_001042492.3(NF1):c.6147+8C>G rs182709912
NM_001042492.3(NF1):c.6393C>T (p.His2131=) rs17881788
NM_001042492.3(NF1):c.6929C>T (p.Pro2310Leu) rs148736217
NM_001042492.3(NF1):c.702G>A (p.Leu234=) rs1801052
NM_001042492.3(NF1):c.7190-5del rs769290414
NM_001042492.3(NF1):c.730+32dup rs71142032
NM_001042492.3(NF1):c.7322-17C>T rs17884859
NM_001042492.3(NF1):c.7368A>G (p.Lys2456=) rs201287021
NM_001042492.3(NF1):c.7461A>G (p.Thr2487=) rs149924365
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.7755C>T (p.Ser2585=) rs17881980
NM_001042492.3(NF1):c.8151G>A (p.Pro2717=) rs2285895
NM_001042492.3(NF1):c.8206G>A (p.Asp2736Asn) rs1597870148
NM_001042492.3(NF1):c.846G>A (p.Gln282=) rs138840528
NM_001042492.3(NF1):c.8499T>C (p.Asn2833=) rs142636150

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