List of variants in gene MYD88 reported as pathogenic for Pyogenic bacterial infections due to MyD88 deficiency

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002468.5(MYD88):c.586C>T (p.Arg196Cys)	rs137853064	0.00001
NM_002468.5(MYD88):c.751C>T (p.Arg251Ter)	rs748659894	0.00001
NC_000003.11:g.(?_38180153)_(38182777_?)del
NM_002468.5(MYD88):c.-24_-6del	rs746651350
NM_002468.5(MYD88):c.103_104del (p.Leu35fs)	rs776336832
NM_002468.5(MYD88):c.154GAG[1] (p.Glu53del)	rs878852993
NM_002468.5(MYD88):c.157G>T (p.Glu53Ter)	rs765198848
NM_002468.5(MYD88):c.256_257del (p.Val86fs)
NM_002468.5(MYD88):c.278T>C (p.Leu93Pro)	rs137853065

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.