ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_030813.6(CLPB):c.668G>A (p.Ser223Asn) rs143097446 0.00471
NM_001258392.3(CLPB):c.1122+16T>C rs187846751 0.00147
NM_001258392.3(CLPB):c.1560+11T>C rs113954132 0.00049
NM_001258392.3(CLPB):c.404-16C>T rs371250603 0.00032
NM_001258392.3(CLPB):c.1425C>T (p.His475=) rs756497518 0.00019
NM_001258392.3(CLPB):c.1429C>T (p.Leu477=) rs77345581 0.00018
NM_001258392.3(CLPB):c.966C>T (p.Ser322=) rs371562971 0.00018
NM_001258392.3(CLPB):c.776-10C>G rs141271919 0.00010
NM_001258392.3(CLPB):c.921C>T (p.Phe307=) rs561993207 0.00007
NM_001258392.3(CLPB):c.1571G>A (p.Arg524Gln) rs576652298 0.00003
NM_001258392.3(CLPB):c.543-12G>C rs750871760 0.00003
NM_001258392.3(CLPB):c.1017C>T (p.Tyr339=) rs772512727
NM_001258392.3(CLPB):c.1066+13_1066+14insTGCT rs1555087616
NM_001258392.3(CLPB):c.1561-18_1561-12del rs1166987571
NM_001258392.3(CLPB):c.1680+7G>A rs1057524470
NM_001258392.3(CLPB):c.651G>A (p.Leu217=) rs375214732
NM_001258392.3(CLPB):c.776-5G>T rs1253919639

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