List of variants in gene MYO9A reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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_006901.4(MYO9A):c.6454G>A (p.Glu2152Lys)	rs74022458	0.00198
NM_006901.4(MYO9A):c.4608A>G (p.Pro1536=)	rs146981046	0.00163
NM_006901.4(MYO9A):c.3429C>T (p.Ile1143=)	rs150655401	0.00162
NM_006901.4(MYO9A):c.3257G>A (p.Arg1086His)	rs75986913	0.00146
NM_006901.4(MYO9A):c.1987-6A>G	rs200246273	0.00081
NM_006901.4(MYO9A):c.4731A>T (p.Leu1577=)	rs142776567	0.00049
NM_006901.4(MYO9A):c.5191A>T (p.Thr1731Ser)	rs142639438	0.00020
NM_006901.4(MYO9A):c.359G>A (p.Ser120Asn)	rs147186127	0.00009
NM_006901.4(MYO9A):c.608A>G (p.Tyr203Cys)	rs374155761	0.00003
NM_006901.4(MYO9A):c.2935A>G (p.Asn979Asp)
NM_006901.4(MYO9A):c.310C>T (p.Arg104Cys)
NM_006901.4(MYO9A):c.3831G>T (p.Met1277Ile)
NM_006901.4(MYO9A):c.6271C>T (p.Leu2091=)	rs1596034423
NM_006901.4(MYO9A):c.6476-7dup	rs574938131

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.