ClinVar Miner

List of variants reported as benign for Hereditary sensory and autonomic neuropathy type IC

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NM_004863.3(SPTLC2):c.*1014C>T rs116563416
NM_004863.3(SPTLC2):c.*1134T>C rs17751562
NM_004863.3(SPTLC2):c.*1221A>G rs80244932
NM_004863.3(SPTLC2):c.*1440G>T rs116702345
NM_004863.3(SPTLC2):c.*1655G>C rs45480297
NM_004863.3(SPTLC2):c.*1709G>A rs146295173
NM_004863.3(SPTLC2):c.*1729G>A rs143610997
NM_004863.3(SPTLC2):c.*1742C>T rs9323644
NM_004863.3(SPTLC2):c.*2159A>G rs45493395
NM_004863.3(SPTLC2):c.*2177A>C rs17824567
NM_004863.3(SPTLC2):c.*2186A>G rs377018367
NM_004863.3(SPTLC2):c.*2302A>G rs11159269
NM_004863.3(SPTLC2):c.*2338G>A rs148034053
NM_004863.3(SPTLC2):c.*2645C>T rs78577388
NM_004863.3(SPTLC2):c.*2699C>A rs142877874
NM_004863.3(SPTLC2):c.*2702G>A rs10147023
NM_004863.3(SPTLC2):c.*2718_*2719delCT rs140918232
NM_004863.3(SPTLC2):c.*2749A>C rs138960830
NM_004863.3(SPTLC2):c.*288C>T rs187745450
NM_004863.3(SPTLC2):c.*2910_*2912del rs145606197
NM_004863.3(SPTLC2):c.*2966G>A rs369681276
NM_004863.3(SPTLC2):c.*3034C>G rs75977251
NM_004863.3(SPTLC2):c.*3224C>T rs77200167
NM_004863.3(SPTLC2):c.*3274C>T rs114274991
NM_004863.3(SPTLC2):c.*3524A>C rs1063270
NM_004863.3(SPTLC2):c.*3526A>T rs530009301
NM_004863.3(SPTLC2):c.*3612T>A rs2364160
NM_004863.3(SPTLC2):c.*3637G>A rs1063271
NM_004863.3(SPTLC2):c.*3812C>T rs74730673
NM_004863.3(SPTLC2):c.*3931G>C rs371265800
NM_004863.3(SPTLC2):c.*397G>T rs140766311
NM_004863.3(SPTLC2):c.*4037G>A rs144430502
NM_004863.3(SPTLC2):c.*4039T>C rs117131683
NM_004863.3(SPTLC2):c.*4089del rs149064904
NM_004863.3(SPTLC2):c.*4131G>A rs45577834
NM_004863.3(SPTLC2):c.*4198C>T rs143542715
NM_004863.3(SPTLC2):c.*4431G>T rs75823402
NM_004863.3(SPTLC2):c.*4446G>T rs11159268
NM_004863.3(SPTLC2):c.*4478C>A rs145218669
NM_004863.3(SPTLC2):c.*4503A>G rs78947178
NM_004863.3(SPTLC2):c.*4645A>G rs10132095
NM_004863.3(SPTLC2):c.*4673_*4674insTG rs58831828
NM_004863.3(SPTLC2):c.*4914C>T rs150007923
NM_004863.3(SPTLC2):c.*523C>T rs561128453
NM_004863.3(SPTLC2):c.*5358T>C rs8021886
NM_004863.3(SPTLC2):c.*5395C>G rs13430
NM_004863.3(SPTLC2):c.*5531A>G rs17105886
NM_004863.3(SPTLC2):c.*6080C>G rs56040359
NM_004863.3(SPTLC2):c.*6253T>C rs370412771
NM_004863.3(SPTLC2):c.*6T>G rs73319080
NM_004863.3(SPTLC2):c.*727C>T rs115976926
NM_004863.3(SPTLC2):c.-181C>G rs538010560
NM_004863.3(SPTLC2):c.-187C>T rs554906103
NM_004863.3(SPTLC2):c.-30G>T rs142320856
NM_004863.3(SPTLC2):c.-42A>G rs751107431
NM_004863.3(SPTLC2):c.-43C>T rs7155278
NM_004863.3(SPTLC2):c.1050C>T (p.Gly350=) rs539265514
NM_004863.3(SPTLC2):c.1128G>A (p.Thr376=) rs773806229
NM_004863.3(SPTLC2):c.1176+7G>A rs74063297
NM_004863.3(SPTLC2):c.117_122del rs577436926
NM_004863.3(SPTLC2):c.1227G>A (p.Thr409=) rs9323646
NM_004863.3(SPTLC2):c.1239T>C (p.Pro413=) rs140041902
NM_004863.3(SPTLC2):c.1247T>C (p.Val416Ala) rs577862696
NM_004863.3(SPTLC2):c.1428T>G (p.Pro476=) rs34418677
NM_004863.3(SPTLC2):c.1449A>T (p.Gly483=) rs149054777
NM_004863.3(SPTLC2):c.1470C>T (p.Asn490=) rs374657234
NM_004863.3(SPTLC2):c.1569+8G>T rs577069180
NM_004863.3(SPTLC2):c.1603T>C (p.Leu535=) rs34017190
NM_004863.3(SPTLC2):c.1614G>A (p.Lys538=) rs143770506
NM_004863.3(SPTLC2):c.162A>C (p.Leu54=) rs115191009
NM_004863.3(SPTLC2):c.1664C>T (p.Thr555Met) rs138652708
NM_004863.3(SPTLC2):c.174G>A (p.Pro58=) rs373828710
NM_004863.3(SPTLC2):c.407G>A (p.Arg136Gln) rs760762454
NM_004863.3(SPTLC2):c.506G>C (p.Gly169Ala) rs75565823
NM_004863.3(SPTLC2):c.561A>G (p.Ser187=) rs143934634
NM_004863.3(SPTLC2):c.612C>T (p.Cys204=) rs115500562
NM_004863.3(SPTLC2):c.723G>A (p.Thr241=) rs114519796
NM_004863.3(SPTLC2):c.723G>T (p.Thr241=) rs114519796
NM_004863.3(SPTLC2):c.761G>C (p.Cys254Ser) rs572378641
NM_004863.3(SPTLC2):c.763C>T (p.Leu255=) rs773905221
NM_004863.3(SPTLC2):c.786T>C (p.Asn262=) rs2364602
NM_004863.3(SPTLC2):c.851-5T>C rs199867946
NM_004863.4(SPTLC2):c.*2375C>T
NM_004863.4(SPTLC2):c.*2962C>T
NM_004863.4(SPTLC2):c.*3666T>G
NM_004863.4(SPTLC2):c.*4030T>G
NM_004863.4(SPTLC2):c.*4108G>A
NM_004863.4(SPTLC2):c.*4276G>A
NM_004863.4(SPTLC2):c.*4842A>C
NM_004863.4(SPTLC2):c.*513C>T
NM_004863.4(SPTLC2):c.*5799C>T
NM_004863.4(SPTLC2):c.*5892C>A

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