ClinVar Miner

List of variants in gene TBC1D24 reported as uncertain significance by Invitae

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Total variants: 71
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HGVS dbSNP
NC_000016.9:g.(?_2546130)_(2550979_?)dup
NM_001199107.2(TBC1D24):c.1015A>G (p.Asn339Asp) rs574768683
NM_001199107.2(TBC1D24):c.1021C>T (p.Arg341Cys)
NM_001199107.2(TBC1D24):c.1022G>A (p.Arg341His) rs754727069
NM_001199107.2(TBC1D24):c.1028A>C (p.Glu343Ala) rs188124777
NM_001199107.2(TBC1D24):c.1039G>A (p.Val347Met) rs371031447
NM_001199107.2(TBC1D24):c.1049T>C (p.Met350Thr) rs1475264921
NM_001199107.2(TBC1D24):c.1072C>A (p.Pro358Thr)
NM_001199107.2(TBC1D24):c.1142+6A>T rs778930581
NM_001199107.2(TBC1D24):c.116C>T (p.Ala39Val) rs773916549
NM_001199107.2(TBC1D24):c.1207-6C>G rs749626631
NM_001199107.2(TBC1D24):c.1271T>G (p.Phe424Cys)
NM_001199107.2(TBC1D24):c.1321C>G (p.Arg441Gly)
NM_001199107.2(TBC1D24):c.1321C>T (p.Arg441Cys)
NM_001199107.2(TBC1D24):c.1322G>A (p.Arg441His)
NM_001199107.2(TBC1D24):c.1327G>C (p.Glu443Gln)
NM_001199107.2(TBC1D24):c.1367C>T (p.Pro456Leu) rs200641000
NM_001199107.2(TBC1D24):c.1411G>A (p.Ala471Thr) rs377448015
NM_001199107.2(TBC1D24):c.1426G>A (p.Ala476Thr)
NM_001199107.2(TBC1D24):c.143A>T (p.His48Leu)
NM_001199107.2(TBC1D24):c.1499C>T (p.Ala500Val) rs564477999
NM_001199107.2(TBC1D24):c.1524C>T (p.Val508=) rs1333624924
NM_001199107.2(TBC1D24):c.1525+6C>T rs758013935
NM_001199107.2(TBC1D24):c.1525G>A (p.Gly509Arg) rs749994791
NM_001199107.2(TBC1D24):c.1544C>T (p.Ala515Val) rs267607105
NM_001199107.2(TBC1D24):c.154G>A (p.Gly52Arg)
NM_001199107.2(TBC1D24):c.1571G>A (p.Arg524Gln)
NM_001199107.2(TBC1D24):c.1577G>A (p.Arg526His) rs752301570
NM_001199107.2(TBC1D24):c.1590C>G (p.Cys530Trp) rs1060502501
NM_001199107.2(TBC1D24):c.1627T>C (p.Phe543Leu) rs1060502502
NM_001199107.2(TBC1D24):c.1641C>A (p.Ala547=) rs553215090
NM_001199107.2(TBC1D24):c.178C>T (p.Arg60Trp) rs373914077
NM_001199107.2(TBC1D24):c.179G>A (p.Arg60Gln) rs200226466
NM_001199107.2(TBC1D24):c.198G>A (p.Thr66=)
NM_001199107.2(TBC1D24):c.217G>A (p.Val73Met)
NM_001199107.2(TBC1D24):c.226G>A (p.Asp76Asn)
NM_001199107.2(TBC1D24):c.244G>T (p.Val82Leu)
NM_001199107.2(TBC1D24):c.28G>A (p.Val10Met)
NM_001199107.2(TBC1D24):c.325C>G (p.Arg109Gly) rs372337277
NM_001199107.2(TBC1D24):c.328G>A (p.Gly110Ser) rs747821285
NM_001199107.2(TBC1D24):c.331G>A (p.Glu111Lys)
NM_001199107.2(TBC1D24):c.344G>A (p.Arg115His) rs201174513
NM_001199107.2(TBC1D24):c.373T>C (p.Phe125Leu) rs1567411503
NM_001199107.2(TBC1D24):c.404C>T (p.Pro135Leu) rs1057519630
NM_001199107.2(TBC1D24):c.405G>A (p.Pro135=) rs778663250
NM_001199107.2(TBC1D24):c.414G>A (p.Val138=) rs1015174831
NM_001199107.2(TBC1D24):c.431A>G (p.Tyr144Cys)
NM_001199107.2(TBC1D24):c.439G>A (p.Asp147Asn) rs267607103
NM_001199107.2(TBC1D24):c.457G>A (p.Glu153Lys) rs376712059
NM_001199107.2(TBC1D24):c.458A>C (p.Glu153Ala)
NM_001199107.2(TBC1D24):c.485A>G (p.Asn162Ser) rs772054145
NM_001199107.2(TBC1D24):c.556C>G (p.Leu186Val) rs1555501245
NM_001199107.2(TBC1D24):c.587A>G (p.Lys196Arg) rs758299397
NM_001199107.2(TBC1D24):c.606G>A (p.Ser202=)
NM_001199107.2(TBC1D24):c.622G>A (p.Val208Ile) rs1355375251
NM_001199107.2(TBC1D24):c.632A>G (p.Asp211Gly)
NM_001199107.2(TBC1D24):c.640C>T (p.Arg214Cys) rs760121083
NM_001199107.2(TBC1D24):c.679C>T (p.Arg227Trp) rs748302886
NM_001199107.2(TBC1D24):c.68G>A (p.Gly23Glu) rs1567410958
NM_001199107.2(TBC1D24):c.725G>A (p.Arg242His)
NM_001199107.2(TBC1D24):c.727G>A (p.Val243Met) rs762660491
NM_001199107.2(TBC1D24):c.731C>A (p.Ala244Glu)
NM_001199107.2(TBC1D24):c.759G>A (p.Lys253=)
NM_001199107.2(TBC1D24):c.793G>A (p.Val265Met) rs772768393
NM_001199107.2(TBC1D24):c.807C>G (p.Ile269Met) rs762576413
NM_001199107.2(TBC1D24):c.808C>T (p.Arg270Cys) rs375860324
NM_001199107.2(TBC1D24):c.817G>A (p.Val273Ile) rs752610561
NM_001199107.2(TBC1D24):c.829G>A (p.Ala277Thr) rs754019727
NM_001199107.2(TBC1D24):c.871G>A (p.Ala291Thr) rs375307187
NM_001199107.2(TBC1D24):c.878G>A (p.Arg293His) rs199700840
NM_001199107.2(TBC1D24):c.920A>G (p.Asn307Ser)

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