ClinVar Miner

List of variants in gene SPRED1 reported as likely benign for not specified

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Total variants: 21
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HGVS dbSNP
NM_152594.3(SPRED1):c.1110C>G (p.Leu370=) rs876657584
NM_152594.3(SPRED1):c.1192G>A (p.Asp398Asn) rs771480941
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe) rs1566877075
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.207+37A>G rs2272105
NM_152594.3(SPRED1):c.211G>A (p.Val71Ile)
NM_152594.3(SPRED1):c.27C>T (p.Asp9=) rs727504717
NM_152594.3(SPRED1):c.306G>A (p.Thr102=) rs372791883
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys) rs201692618
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.583-7A>G rs115970207
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.702C>G (p.Ile234Met) rs138553244
NM_152594.3(SPRED1):c.703A>C (p.Arg235=) rs1177047281
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635
NM_152594.3(SPRED1):c.938C>T (p.Thr313Met) rs766814966
NM_152594.3(SPRED1):c.990T>G (p.Gly330=)

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