List of variants in gene CLPB reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_001258392.3(CLPB):c.456-4731G>T	rs4943891	0.79437
NM_001258392.3(CLPB):c.1786-176C>T	rs12793524	0.39577
NM_001258392.3(CLPB):c.775+50T>G	rs545388830	0.26318
NM_001258392.3(CLPB):c.1330-285C>G	rs474629	0.20258
NM_001258392.3(CLPB):c.1786-55A>G	rs680660	0.18047
NM_001258392.3(CLPB):c.874-346A>G	rs60024067	0.10300
NM_001258392.3(CLPB):c.1486+142G>A	rs590732	0.09940
NM_001258392.3(CLPB):c.840A>G (p.Glu280=)	rs36049191	0.09452
NM_001258392.3(CLPB):c.646+97A>G	rs3741162	0.07598
NM_001258392.3(CLPB):c.456-135C>A	rs74714550	0.04700
NM_030813.5(CLPB):c.-213C>T	rs74895347	0.03991
NM_001258392.3(CLPB):c.776-62G>C	rs59514150	0.03950
NM_001258392.3(CLPB):c.646+6968T>C	rs117652953	0.03005
NC_000011.10:g.72434676A>C	rs7950298	0.02998
NM_001258392.3(CLPB):c.988+145T>C	rs117954624	0.02885
NM_001258392.3(CLPB):c.1067-174G>A	rs118089225	0.02870
NM_001258392.3(CLPB):c.646+188del	rs144832068	0.02812
NM_001258392.3(CLPB):c.543-290T>A	rs57936278	0.02014
NM_001258392.3(CLPB):c.1860C>T (p.Arg620=)	rs35401939	0.02006
NM_001258392.3(CLPB):c.794G>C (p.Arg265Thr)	rs7938203	0.01762
NM_001258392.3(CLPB):c.456-5456T>A	rs147128418	0.01649
NM_001258392.3(CLPB):c.996G>A (p.Arg332=)	rs146912721	0.00764
NM_001258392.3(CLPB):c.2026A>G (p.Thr676Ala)	rs112524097	0.00471
NM_030813.6(CLPB):c.668G>A (p.Ser223Asn)	rs143097446	0.00471
NM_001258392.3(CLPB):c.1993C>T (p.Arg665Trp)	rs141383303	0.00324
NM_030813.6(CLPB):c.661G>A (p.Gly221Ser)	rs150552809	0.00247
NM_001258392.3(CLPB):c.1535A>T (p.Glu512Val)	rs373383193	0.00005
NC_000011.10:g.72434827_72434828del	rs757349340
NM_001258392.3(CLPB):c.1487-248_1487-244del	rs72333851
NM_001258392.3(CLPB):c.1487-251_1487-245dup	rs149822834
NM_001258392.3(CLPB):c.1680+78CA[5]	rs59806404
NM_001258392.3(CLPB):c.456-4751G>C	rs7947973
NM_001258392.3(CLPB):c.456-4797C>T	rs113165548
NM_001258392.3(CLPB):c.776-273C>T	rs117992720

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