ClinVar Miner

List of variants in gene SDHAF2 studied for adrenal gland disease

Included ClinVar conditions (124):
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Gene type:
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Total variants: 105
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HGVS dbSNP
NC_000011.9:g.(?_61205087)_(61213553_?)dup
NM_017841.2(SDHAF2):c.*113C>A rs886048416
NM_017841.2(SDHAF2):c.*12C>T rs113652589
NM_017841.2(SDHAF2):c.*170C>A rs886048417
NM_017841.2(SDHAF2):c.*172delA rs537244040
NM_017841.2(SDHAF2):c.*233C>T rs886048419
NM_017841.2(SDHAF2):c.*377T>C rs17702
NM_017841.2(SDHAF2):c.*378G>A rs7935377
NM_017841.2(SDHAF2):c.*389C>T rs886048420
NM_017841.2(SDHAF2):c.*415A>G rs61132686
NM_017841.2(SDHAF2):c.*446C>G rs886048421
NM_017841.2(SDHAF2):c.*456A>G rs6632
NM_017841.2(SDHAF2):c.*49A>G rs549312009
NM_017841.2(SDHAF2):c.*58G>A rs754124809
NM_017841.2(SDHAF2):c.*627G>T rs886048422
NM_017841.2(SDHAF2):c.*653A>G rs886048423
NM_017841.2(SDHAF2):c.*669A>G rs747631379
NM_017841.2(SDHAF2):c.*76C>T rs112750991
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)
NM_017841.2(SDHAF2):c.130_132del (p.Gln44del)
NM_017841.2(SDHAF2):c.133A>G (p.Lys45Glu) rs368945911
NM_017841.2(SDHAF2):c.136G>A (p.Asp46Asn)
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)
NM_017841.2(SDHAF2):c.156G>A (p.Leu52=) rs773466310
NM_017841.2(SDHAF2):c.157C>T (p.Pro53Ser) rs1060503390
NM_017841.2(SDHAF2):c.15A>G (p.Thr5=) rs144511254
NM_017841.2(SDHAF2):c.165G>A (p.Trp55Ter) rs774508076
NM_017841.2(SDHAF2):c.177dup (p.Asp60Ter) rs1554984631
NM_017841.2(SDHAF2):c.194C>T (p.Thr65Ile)
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.21C>T (p.Phe7=) rs892955355
NM_017841.2(SDHAF2):c.221G>A (p.Ser74Asn) rs1060503389
NM_017841.2(SDHAF2):c.232G>A (p.Gly78Arg) rs113560320
NM_017841.2(SDHAF2):c.239T>C (p.Leu80Ser) rs376560419
NM_017841.2(SDHAF2):c.240G>A (p.Leu80=) rs1223446048
NM_017841.2(SDHAF2):c.248G>T (p.Cys83Phe) rs982336783
NM_017841.2(SDHAF2):c.253C>A (p.Leu85Ile)
NM_017841.2(SDHAF2):c.25A>G (p.Thr9Ala) rs1554983610
NM_017841.2(SDHAF2):c.260+1G>A rs749527870
NM_017841.2(SDHAF2):c.261-2A>T
NM_017841.2(SDHAF2):c.261-9delT rs1060504900
NM_017841.2(SDHAF2):c.264T>G (p.Leu88=) rs1554984669
NM_017841.2(SDHAF2):c.294A>G (p.Thr98=) rs762441285
NM_017841.2(SDHAF2):c.29C>T (p.Ser10Leu)
NM_017841.2(SDHAF2):c.2T>C (p.Met1Thr) rs1060503392
NM_017841.2(SDHAF2):c.305_306insA (p.Asn103fs) rs753554501
NM_017841.2(SDHAF2):c.313T>A (p.Tyr105Asn) rs1485358364
NM_017841.2(SDHAF2):c.314A>G (p.Tyr105Cys)
NM_017841.2(SDHAF2):c.319C>T (p.Arg107Cys) rs140191819
NM_017841.2(SDHAF2):c.320G>A (p.Arg107His) rs535627239
NM_017841.2(SDHAF2):c.327T>A (p.Ile109=) rs757670376
NM_017841.2(SDHAF2):c.327T>G (p.Ile109Met)
NM_017841.2(SDHAF2):c.32C>T (p.Ser11Leu) rs148425779
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)
NM_017841.2(SDHAF2):c.347G>A (p.Trp116Ter) rs876658350
NM_017841.2(SDHAF2):c.348G>C (p.Trp116Cys)
NM_017841.2(SDHAF2):c.350A>T (p.Asp117Val)
NM_017841.2(SDHAF2):c.355dup (p.Tyr119fs) rs1456129845
NM_017841.2(SDHAF2):c.35T>C (p.Leu12Pro)
NM_017841.2(SDHAF2):c.36+10G>A rs114207859
NM_017841.2(SDHAF2):c.36+5G>A
NM_017841.2(SDHAF2):c.37-7A>G rs1554984610
NM_017841.2(SDHAF2):c.370+12G>A rs886048415
NM_017841.2(SDHAF2):c.370+4C>G
NM_017841.2(SDHAF2):c.370+6G>A rs1565128722
NM_017841.2(SDHAF2):c.370+8G>C rs764742919
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)
NM_017841.2(SDHAF2):c.415C>A (p.Leu139Met) rs1565130851
NM_017841.2(SDHAF2):c.427T>A (p.Phe143Ile)
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)
NM_017841.2(SDHAF2):c.453G>A (p.Gln151=) rs1271900425
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.465C>T (p.Ala155=) rs758154733
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.63A>G (p.Leu21=) rs191513932
NM_017841.2(SDHAF2):c.6G>A (p.Ala2=) rs747571875
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.97C>T (p.Arg33Cys) rs144867876
NM_017841.2(SDHAF2):c.98G>A (p.Arg33His) rs777442412
NM_017841.2(SDHAF2):c.98G>T (p.Arg33Leu)

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