ClinVar Miner

List of variants in gene SPRED1 reported as likely benign by GeneDx

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Gene type:
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Total variants: 18
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HGVS dbSNP
NM_152594.3(SPRED1):c.1176G>A (p.Ser392=) rs755223172
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe) rs1566877075
NM_152594.3(SPRED1):c.207+15A>G rs377288061
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475
NM_152594.3(SPRED1):c.33-11A>G rs775671940
NM_152594.3(SPRED1):c.376+3A>T rs775985211
NM_152594.3(SPRED1):c.377-10A>G rs376134678
NM_152594.3(SPRED1):c.384C>T (p.Pro128=) rs761058615
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile) rs147474792
NM_152594.3(SPRED1):c.594T>C (p.Gly198=) rs756643495
NM_152594.3(SPRED1):c.636A>C (p.Val212=) rs1057523137
NM_152594.3(SPRED1):c.703A>C (p.Arg235=) rs1177047281
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635
NM_152594.3(SPRED1):c.933T>C (p.Phe311=) rs1057522873
NM_152594.3(SPRED1):c.938C>T (p.Thr313Met) rs766814966
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874
NM_152594.3(SPRED1):c.963G>A (p.Lys321=) rs369711772

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