List of variants in gene CLPB reported as benign for not provided

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

Download table as spreadsheet

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.1935C>T (p.Leu645=)	rs138717332	0.00088
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.