List of variants in gene MYO3A reported by Fulgent Genetics, Fulgent Genetics

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017433.5(MYO3A):c.533C>T (p.Thr178Ile)	rs33968748	0.01220
NM_017433.5(MYO3A):c.3094G>A (p.Ala1032Thr)	rs34918608	0.00845
NM_017433.5(MYO3A):c.170A>C (p.Asp57Ala)	rs146511800	0.00094
NM_017433.5(MYO3A):c.113T>C (p.Val38Ala)	rs144518447	0.00041
NM_017433.5(MYO3A):c.2275A>T (p.Asn759Tyr)	rs201033926	0.00030
NM_017433.5(MYO3A):c.4840C>T (p.Gln1614Ter)	rs146106052	0.00022
NM_017433.5(MYO3A):c.656C>T (p.Thr219Met)	rs377660409	0.00017
NM_017433.5(MYO3A):c.1828A>G (p.Ile610Val)	rs151254539	0.00013
NM_017433.5(MYO3A):c.2870A>G (p.Glu957Gly)	rs764192576
NM_017433.5(MYO3A):c.4567C>G (p.Arg1523Gly)	rs727504688

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.