List of variants in gene CLPB reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001258392.3(CLPB):c.1792C>T (p.Arg598Cys)	rs150343959	0.00133
NM_001258392.3(CLPB):c.1760A>G (p.Tyr587Cys)	rs786205138	0.00003
NM_001258392.3(CLPB):c.713C>T (p.Thr238Met)	rs200032855	0.00003
NM_001258392.3(CLPB):c.1073C>A (p.Thr358Lys)	rs2135510485
NM_001258392.3(CLPB):c.1588G>A (p.Gly530Arg)	rs2135485868
NM_001258392.3(CLPB):c.1591C>G (p.Arg531Gly)	rs1949512456
NM_001258392.3(CLPB):c.1591C>T (p.Arg531Trp)	rs1949512456
NM_001258392.3(CLPB):c.1592G>A (p.Arg531Gln)	rs1590753221
NM_001258392.3(CLPB):c.1595del (p.Ile532fs)	rs876657402
NM_001258392.3(CLPB):c.1682C>T (p.Ala561Val)	rs748010262
NM_001258392.3(CLPB):c.1768C>T (p.Arg590Cys)	rs2135484821
NM_001258392.3(CLPB):c.1813_1814delinsAA (p.Ala605Lys)
NM_001258392.3(CLPB):c.1847G>T (p.Gly616Val)	rs759500860
NM_001258392.3(CLPB):c.871A>T (p.Lys291Ter)	rs786205139

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