ClinVar Miner

List of variants in gene TBC1D24 reported as uncertain significance for not specified

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Total variants: 30
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HGVS dbSNP
NC_000016.10:g.2496278T>C
NM_001199107.2(TBC1D24):c.*2G>A rs780054979
NM_001199107.2(TBC1D24):c.-4C>T rs202124579
NM_001199107.2(TBC1D24):c.1015A>G (p.Asn339Asp) rs574768683
NM_001199107.2(TBC1D24):c.1026G>A (p.Ser342=) rs370244846
NM_001199107.2(TBC1D24):c.1028A>C (p.Glu343Ala) rs188124777
NM_001199107.2(TBC1D24):c.1143-15G>A rs371213803
NM_001199107.2(TBC1D24):c.116C>A (p.Ala39Glu) rs773916549
NM_001199107.2(TBC1D24):c.1196C>T (p.Thr399Met) rs61731477
NM_001199107.2(TBC1D24):c.1327G>A (p.Glu443Lys) rs141399869
NM_001199107.2(TBC1D24):c.1457G>A (p.Arg486His) rs796053405
NM_001199107.2(TBC1D24):c.1475C>T (p.Ser492Phe) rs1249590916
NM_001199107.2(TBC1D24):c.1490T>C (p.Met497Thr) rs367710709
NM_001199107.2(TBC1D24):c.1529G>A (p.Gly510Glu) rs755880523
NM_001199107.2(TBC1D24):c.1558G>C (p.Gly520Arg) rs1555501693
NM_001199107.2(TBC1D24):c.1576C>T (p.Arg526Cys) rs767145914
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met) rs201649140
NM_001199107.2(TBC1D24):c.169C>T (p.Arg57Cys) rs202162520
NM_001199107.2(TBC1D24):c.344G>A (p.Arg115His) rs201174513
NM_001199107.2(TBC1D24):c.439G>A (p.Asp147Asn) rs267607103
NM_001199107.2(TBC1D24):c.485A>G (p.Asn162Ser) rs772054145
NM_001199107.2(TBC1D24):c.554_559del (p.Asp185_Leu186del) rs1215641557
NM_001199107.2(TBC1D24):c.621G>C (p.Gln207His) rs876658012
NM_001199107.2(TBC1D24):c.641G>A (p.Arg214His) rs200324356
NM_001199107.2(TBC1D24):c.731C>T (p.Ala244Val) rs375873110
NM_001199107.2(TBC1D24):c.776C>A (p.Pro259Gln) rs779398267
NM_001199107.2(TBC1D24):c.836C>T (p.Thr279Met) rs779234824
NM_001199107.2(TBC1D24):c.845C>G (p.Pro282Arg) rs747538224
NM_001199107.2(TBC1D24):c.878G>A (p.Arg293His) rs199700840
NM_001199107.2(TBC1D24):c.965+38T>G rs571500991

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