ClinVar Miner

List of variants in gene NF2 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP
NM_000268.3(NF2):c.1000-4G>A rs200113152
NM_000268.3(NF2):c.1020T>C (p.Ala340=) rs1556000130
NM_000268.3(NF2):c.1056G>A (p.Thr352=) rs145427713
NM_000268.3(NF2):c.1077G>A (p.Arg359=) rs878853923
NM_000268.3(NF2):c.1128G>C (p.Arg376=) rs757322524
NM_000268.3(NF2):c.1206C>T (p.Ala402=) rs137953976
NM_000268.3(NF2):c.1209A>G (p.Ala403=) rs1026655770
NM_000268.3(NF2):c.1215T>G (p.Ala405=) rs772219612
NM_000268.3(NF2):c.1248G>A (p.Ala416=) rs759993776
NM_000268.3(NF2):c.1273C>T (p.Leu425=) rs142446775
NM_000268.3(NF2):c.1290G>A (p.Val430=) rs756041768
NM_000268.3(NF2):c.1311A>G (p.Ala437=) rs144628209
NM_000268.3(NF2):c.1317G>A (p.Lys439=) rs1556000937
NM_000268.3(NF2):c.1323T>A (p.Ala441=) rs1556000942
NM_000268.3(NF2):c.1387G>A (p.Glu463Lys) rs74315503
NM_000268.3(NF2):c.1392G>A (p.Ala464=) rs375819833
NM_000268.3(NF2):c.1470G>A (p.Pro490=) rs373442542
NM_000268.3(NF2):c.1491C>T (p.Ser497=) rs1556002514
NM_000268.3(NF2):c.1494C>T (p.Phe498=) rs1060504990
NM_000268.3(NF2):c.1500C>T (p.Leu500=) rs758182356
NM_000268.3(NF2):c.1548G>T (p.Arg516=) rs534398531
NM_000268.3(NF2):c.1575-5G>A rs199622889
NM_000268.3(NF2):c.1617C>T (p.Leu539=) rs1556003665
NM_000268.3(NF2):c.1638C>T (p.Ile546=) rs774264046
NM_000268.3(NF2):c.1639G>A (p.Glu547Lys) rs199669486
NM_000268.3(NF2):c.1671T>C (p.Ala557=) rs759780271
NM_000268.3(NF2):c.1698C>T (p.Ser566=) rs751987156
NM_000268.3(NF2):c.1722C>T (p.His574=) rs1041539951
NM_000268.3(NF2):c.1749G>A (p.Gln583=) rs201911915
NM_000268.3(NF2):c.1753G>A (p.Ala585Thr) rs145446060
NM_000268.3(NF2):c.255T>C (p.Asp85=) rs375802248
NM_000268.3(NF2):c.294C>G (p.Ala98=) rs1555987671
NM_000268.3(NF2):c.325C>T (p.Leu109=) rs201603384
NM_000268.3(NF2):c.354C>T (p.Phe118=) rs756564761
NM_000268.3(NF2):c.364-9T>C rs767658752
NM_000268.3(NF2):c.447+15_447+17delGAA rs1555988797
NM_000268.3(NF2):c.448-4C>G rs760733256
NM_000268.3(NF2):c.448-5T>C rs878853928
NM_000268.3(NF2):c.459C>T (p.Tyr153=) rs142972020
NM_000268.3(NF2):c.465C>T (p.Pro155=) rs374911526
NM_000268.3(NF2):c.48G>A (p.Arg16=) rs774973059
NM_000268.3(NF2):c.517-4G>A rs1165155285
NM_000268.3(NF2):c.543G>A (p.Pro181=) rs139838280
NM_000268.3(NF2):c.576C>T (p.Tyr192=) rs149803133
NM_000268.3(NF2):c.579A>G (p.Ala193=) rs1332985565
NM_000268.3(NF2):c.600-6C>T rs749155274
NM_000268.3(NF2):c.771G>A (p.Pro257=) rs759032771
NM_000268.3(NF2):c.783C>T (p.Ile261=) rs765223726
NM_000268.3(NF2):c.789C>T (p.Asn263=) rs1555996218
NM_000268.3(NF2):c.798C>T (p.Tyr266=) rs917257652
NM_000268.3(NF2):c.849C>T (p.Phe283=) rs1555997567
NM_000268.3(NF2):c.861C>T (p.Ser287=) rs143160499
NM_000268.3(NF2):c.879T>C (p.Asn293=) rs151198477
NM_000268.3(NF2):c.882G>A (p.Lys294=) rs146166875
NM_000268.3(NF2):c.885+10G>C rs369317112
NM_000268.3(NF2):c.903C>T (p.Ile301=) rs199957176
NM_000268.3(NF2):c.912T>C (p.His304=) rs200272173
NM_000268.3(NF2):c.966A>G (p.Lys322=) rs746175548

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