ClinVar Miner

List of variants in gene SPRED1 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_152594.3(SPRED1):c.-12G>T rs371200183
NM_152594.3(SPRED1):c.1044T>C (p.Val348=) rs3751526
NM_152594.3(SPRED1):c.1108C>T (p.Leu370Phe) rs397517870
NM_152594.3(SPRED1):c.1110C>G (p.Leu370=) rs876657584
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964
NM_152594.3(SPRED1):c.177T>C (p.Phe59=) rs397517871
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475
NM_152594.3(SPRED1):c.27C>T (p.Asp9=) rs727504717
NM_152594.3(SPRED1):c.291G>A (p.Lys97=) rs7182445
NM_152594.3(SPRED1):c.377-10A>G rs376134678
NM_152594.3(SPRED1):c.423+2T>C rs1555391161
NM_152594.3(SPRED1):c.424-5A>G rs752656697
NM_152594.3(SPRED1):c.424-8C>A rs7180446
NM_152594.3(SPRED1):c.583-7A>G rs115970207
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile) rs147474792
NM_152594.3(SPRED1):c.675C>T (p.Ser225=) rs144764225
NM_152594.3(SPRED1):c.702C>G (p.Ile234Met) rs138553244
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874

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