ClinVar Miner

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

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Gene type:
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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635 0.00204
NM_152594.3(SPRED1):c.702C>G (p.Ile234Met) rs138553244 0.00074
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys) rs201692618 0.00042
NM_152594.3(SPRED1):c.377-10A>G rs376134678 0.00026
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964 0.00017
NM_152594.3(SPRED1):c.376+3A>T rs775985211 0.00015
NM_152594.3(SPRED1):c.938C>T (p.Thr313Met) rs766814966 0.00013
NM_152594.3(SPRED1):c.177T>C (p.Phe59=) rs397517871 0.00010
NM_152594.3(SPRED1):c.1192G>A (p.Asp398Asn) rs771480941 0.00009
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile) rs147474792 0.00008
NM_152594.3(SPRED1):c.594T>C (p.Gly198=) rs756643495 0.00004
NM_152594.3(SPRED1):c.306G>A (p.Thr102=) rs372791883 0.00003
NM_152594.3(SPRED1):c.42T>C (p.Tyr14=) rs764234046 0.00003
NM_152594.3(SPRED1):c.1191C>T (p.Asp397=) rs749745659 0.00001
NM_152594.3(SPRED1):c.15G>C (p.Thr5=) rs1278027767 0.00001
NM_152594.3(SPRED1):c.211G>A (p.Val71Ile) rs369150309 0.00001
NM_152594.3(SPRED1):c.27C>T (p.Asp9=) rs727504717 0.00001
NM_152594.3(SPRED1):c.33-11A>G rs775671940 0.00001
NM_152594.3(SPRED1):c.60G>C (p.Val20=) rs367745143 0.00001
NM_152594.3(SPRED1):c.954A>G (p.Leu318=) rs753357510 0.00001
NM_152594.3(SPRED1):c.990T>G (p.Gly330=) rs1184835258 0.00001
NM_152594.3(SPRED1):c.1110C>G (p.Leu370=) rs876657584
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe)
NM_152594.3(SPRED1):c.1299T>C (p.Cys433=) rs2141016779
NM_152594.3(SPRED1):c.207+37A>G rs2272105
NM_152594.3(SPRED1):c.703A>C (p.Arg235=) rs1177047281
NM_152594.3(SPRED1):c.999T>C (p.Ser333=)

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