List of variants in gene PLCB1 reported as likely benign for not specified

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_015192.4(PLCB1):c.102C>T (p.Asp34=)	rs16994453	0.18027
NM_015192.4(PLCB1):c.1251-4T>G	rs2076689	0.09450
NM_015192.4(PLCB1):c.2082G>A (p.Gly694=)	rs3761170	0.05661
NM_015192.4(PLCB1):c.2199G>A (p.Val733=)	rs8118206	0.01438
NM_015192.4(PLCB1):c.2191C>G (p.Pro731Ala)	rs61755434	0.00997
NM_015192.4(PLCB1):c.2413+9C>T	rs138442805	0.00934
NM_015192.4(PLCB1):c.1469A>G (p.Tyr490Cys)	rs45608240	0.00391
NM_015192.4(PLCB1):c.3550C>T (p.Leu1184Phe)	rs28390202	0.00270
NM_015192.4(PLCB1):c.2673T>G (p.Pro891=)	rs142813933	0.00260
NM_015192.4(PLCB1):c.3120A>G (p.Gln1040=)	rs61755436	0.00213
NM_015192.4(PLCB1):c.2711-18C>T	rs186797959	0.00181
NM_015192.4(PLCB1):c.1491C>T (p.Phe497=)	rs145869401	0.00110
NM_015192.4(PLCB1):c.3039G>A (p.Gln1013=)	rs139859188	0.00049
NM_015192.4(PLCB1):c.3584A>G (p.His1195Arg)	rs186429469	0.00016

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.