ClinVar Miner

List of variants in gene SDHAF2 reported as uncertain significance for Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Gene type:
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Total variants: 117
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HGVS dbSNP
NC_000011.10:g.(?_61437615)_(61446071_?)dup
NC_000011.10:g.61430118G>A
NC_000011.9:g.(?_61205087)_(61213553_?)dup
NM_017841.2(SDHAF2):c.*233C>T rs886048419
NM_017841.2(SDHAF2):c.*389C>T rs886048420
NM_017841.2(SDHAF2):c.*446C>G rs886048421
NM_017841.2(SDHAF2):c.*58G>A rs754124809
NM_017841.2(SDHAF2):c.*669A>G rs747631379
NM_017841.2(SDHAF2):c.106A>G (p.Arg36Gly) rs1413272315
NM_017841.2(SDHAF2):c.109G>T (p.Gly37Cys) rs868016844
NM_017841.2(SDHAF2):c.11C>G (p.Ser4Cys) rs778449586
NM_017841.2(SDHAF2):c.130_132del (p.Gln44del) rs1590764793
NM_017841.2(SDHAF2):c.133A>G (p.Lys45Glu) rs368945911
NM_017841.2(SDHAF2):c.136G>A (p.Asp46Asn) rs1590764803
NM_017841.2(SDHAF2):c.138C>G (p.Asp46Glu) rs969049910
NM_017841.2(SDHAF2):c.139A>G (p.Met47Val) rs111402137
NM_017841.2(SDHAF2):c.13A>G (p.Thr5Ala) rs775763888
NM_017841.2(SDHAF2):c.145_147del (p.Glu49del) rs749431351
NM_017841.2(SDHAF2):c.157C>T (p.Pro53Ser) rs1060503390
NM_017841.2(SDHAF2):c.158C>T (p.Pro53Leu) rs562958122
NM_017841.2(SDHAF2):c.194C>T (p.Thr65Ile) rs752462796
NM_017841.2(SDHAF2):c.205C>T (p.Arg69Cys) rs532255760
NM_017841.2(SDHAF2):c.206G>A (p.Arg69His) rs753474292
NM_017841.2(SDHAF2):c.218A>C (p.Glu73Ala) rs1554984643
NM_017841.2(SDHAF2):c.221G>A (p.Ser74Asn) rs1060503389
NM_017841.2(SDHAF2):c.239T>C (p.Leu80Ser) rs376560419
NM_017841.2(SDHAF2):c.248G>T (p.Cys83Phe) rs982336783
NM_017841.2(SDHAF2):c.253C>A (p.Leu85Ile) rs1300112394
NM_017841.2(SDHAF2):c.25A>G (p.Thr9Ala) rs1554983610
NM_017841.2(SDHAF2):c.260+3A>G rs1445986287
NM_017841.2(SDHAF2):c.286C>T (p.His96Tyr) rs755605816
NM_017841.2(SDHAF2):c.29C>T (p.Ser10Leu) rs1590759653
NM_017841.2(SDHAF2):c.2T>C (p.Met1Thr) rs1060503392
NM_017841.2(SDHAF2):c.313T>A (p.Tyr105Asn) rs1485358364
NM_017841.2(SDHAF2):c.314A>G (p.Tyr105Cys) rs1402726087
NM_017841.2(SDHAF2):c.327T>G (p.Ile109Met) rs757670376
NM_017841.2(SDHAF2):c.330C>A (p.Asn110Lys) rs779335034
NM_017841.2(SDHAF2):c.331G>A (p.Glu111Lys) rs145616631
NM_017841.2(SDHAF2):c.341A>G (p.Asn114Ser) rs747022200
NM_017841.2(SDHAF2):c.347G>A (p.Trp116Ter) rs876658350
NM_017841.2(SDHAF2):c.348G>C (p.Trp116Cys) rs1590765145
NM_017841.2(SDHAF2):c.350A>T (p.Asp117Val) rs151040226
NM_017841.2(SDHAF2):c.355dup (p.Tyr119fs) rs1456129845
NM_017841.2(SDHAF2):c.35T>C (p.Leu12Pro) rs1590759677
NM_017841.2(SDHAF2):c.36+5G>A rs1590759705
NM_017841.2(SDHAF2):c.370+4C>G rs758935566
NM_017841.2(SDHAF2):c.370+6G>A rs1565128722
NM_017841.2(SDHAF2):c.370G>A (p.Glu124Lys) rs1237175697
NM_017841.2(SDHAF2):c.371-2A>G rs375280597
NM_017841.2(SDHAF2):c.37A>T (p.Met13Leu) rs1361460244
NM_017841.2(SDHAF2):c.383C>T (p.Ala128Val) rs1554985400
NM_017841.2(SDHAF2):c.385C>T (p.Pro129Ser) rs1060503391
NM_017841.2(SDHAF2):c.391A>T (p.Ile131Leu) rs773580529
NM_017841.2(SDHAF2):c.410T>A (p.Met137Lys) rs367574730
NM_017841.2(SDHAF2):c.415C>A (p.Leu139Met) rs1565130851
NM_017841.2(SDHAF2):c.427T>A (p.Phe143Ile) rs755233768
NM_017841.2(SDHAF2):c.430G>A (p.Ala144Thr) rs572576746
NM_017841.2(SDHAF2):c.43G>T (p.Ala15Ser) rs1002894711
NM_017841.2(SDHAF2):c.446_447del (p.Lys149fs) rs772219112
NM_017841.2(SDHAF2):c.449A>G (p.Glu150Gly) rs1363376859
NM_017841.2(SDHAF2):c.458T>C (p.Leu153Pro) rs753711279
NM_017841.2(SDHAF2):c.460C>T (p.Arg154Cys) rs778585796
NM_017841.2(SDHAF2):c.464C>T (p.Ala155Val) rs1245083102
NM_017841.2(SDHAF2):c.476A>C (p.Glu159Ala) rs140920079
NM_017841.2(SDHAF2):c.490A>G (p.Lys164Glu) rs150187184
NM_017841.2(SDHAF2):c.496C>T (p.Arg166Cys) rs968303021
NM_017841.2(SDHAF2):c.497G>A (p.Arg166His) rs768048172
NM_017841.2(SDHAF2):c.52A>G (p.Arg18Gly) rs200911550
NM_017841.2(SDHAF2):c.60C>A (p.Ser20Arg) rs1565128479
NM_017841.2(SDHAF2):c.7G>T (p.Val3Leu) rs149277592
NM_017841.2(SDHAF2):c.80G>A (p.Ser27Asn) rs759472787
NM_017841.2(SDHAF2):c.98G>A (p.Arg33His) rs777442412
NM_017841.2(SDHAF2):c.98G>T (p.Arg33Leu) rs777442412
NM_017841.4(SDHAF2):c.*284C>T
NM_017841.4(SDHAF2):c.*476C>T
NM_017841.4(SDHAF2):c.*479A>G
NM_017841.4(SDHAF2):c.*661A>G
NM_017841.4(SDHAF2):c.100T>C (p.Phe34Leu)
NM_017841.4(SDHAF2):c.101T>C (p.Phe34Ser)
NM_017841.4(SDHAF2):c.103T>C (p.Tyr35His)
NM_017841.4(SDHAF2):c.121A>G (p.Thr41Ala)
NM_017841.4(SDHAF2):c.146A>G (p.Glu49Gly)
NM_017841.4(SDHAF2):c.14C>T (p.Thr5Ile)
NM_017841.4(SDHAF2):c.169G>A (p.Glu57Lys)
NM_017841.4(SDHAF2):c.17T>C (p.Val6Ala)
NM_017841.4(SDHAF2):c.190G>A (p.Glu64Lys)
NM_017841.4(SDHAF2):c.206G>T (p.Arg69Leu)
NM_017841.4(SDHAF2):c.208C>G (p.Leu70Val)
NM_017841.4(SDHAF2):c.215A>G (p.Tyr72Cys)
NM_017841.4(SDHAF2):c.222C>G (p.Ser74Arg)
NM_017841.4(SDHAF2):c.235A>G (p.Met79Val) rs781702725
NM_017841.4(SDHAF2):c.246C>G (p.Asn82Lys) rs1590764924
NM_017841.4(SDHAF2):c.265T>C (p.Phe89Leu)
NM_017841.4(SDHAF2):c.274G>A (p.Glu92Lys)
NM_017841.4(SDHAF2):c.279T>G (p.His93Gln)
NM_017841.4(SDHAF2):c.334C>A (p.Pro112Thr)
NM_017841.4(SDHAF2):c.337A>G (p.Ser113Gly)
NM_017841.4(SDHAF2):c.350A>G (p.Asp117Gly) rs151040226
NM_017841.4(SDHAF2):c.352A>G (p.Ile118Val) rs747994812
NM_017841.4(SDHAF2):c.370+2T>A
NM_017841.4(SDHAF2):c.37A>G (p.Met13Val)
NM_017841.4(SDHAF2):c.3G>A (p.Met1Ile)
NM_017841.4(SDHAF2):c.406G>A (p.Val136Ile)
NM_017841.4(SDHAF2):c.410T>G (p.Met137Arg)
NM_017841.4(SDHAF2):c.436AACAAA[1] (p.146NK[1])
NM_017841.4(SDHAF2):c.43G>C (p.Ala15Pro)
NM_017841.4(SDHAF2):c.443del (p.Asn148fs) rs1002286076
NM_017841.4(SDHAF2):c.444_447del (p.Asn148fs)
NM_017841.4(SDHAF2):c.446A>C (p.Lys149Thr)
NM_017841.4(SDHAF2):c.446A>G (p.Lys149Arg)
NM_017841.4(SDHAF2):c.451C>T (p.Gln151Ter)
NM_017841.4(SDHAF2):c.461G>A (p.Arg154His) rs768954974
NM_017841.4(SDHAF2):c.46C>G (p.Leu16Val)
NM_017841.4(SDHAF2):c.473T>C (p.Leu158Pro)
NM_017841.4(SDHAF2):c.83T>G (p.Val28Gly)
NM_017841.4(SDHAF2):c.8T>C (p.Val3Ala)
NM_017841.4(SDHAF2):c.96A>T (p.Arg32Ser)

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