List of variants in gene MYO15A reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.1111C>A (p.Pro371Thr)	rs200382813	0.00153
NM_016239.4(MYO15A):c.2194C>T (p.Pro732Ser)	rs376451611	0.00132
NM_016239.4(MYO15A):c.5060C>T (p.Pro1687Leu)	rs58625281	0.00087
NM_016239.4(MYO15A):c.3196G>C (p.Ala1066Pro)	rs199537186	0.00073
NM_016239.4(MYO15A):c.877G>A (p.Asp293Asn)	rs201415651	0.00051
NM_016239.4(MYO15A):c.3659G>A (p.Gly1220Glu)	rs201689819	0.00036
NM_016239.4(MYO15A):c.4976G>A (p.Arg1659Gln)	rs141473928	0.00035
NM_016239.4(MYO15A):c.10394G>A (p.Arg3465Gln)	rs199783506	0.00026
NM_016239.4(MYO15A):c.9620G>A (p.Arg3207His)	rs199621031	0.00026
NM_016239.4(MYO15A):c.10054G>A (p.Ala3352Thr)	rs367863299	0.00013
NM_016239.4(MYO15A):c.3743G>A (p.Arg1248Gln)	rs751800816	0.00003
NM_016239.4(MYO15A):c.1672G>A (p.Gly558Ser)	rs761888570	0.00002
NM_016239.4(MYO15A):c.2099A>T (p.His700Leu)	rs1042721945	0.00002
NM_016239.4(MYO15A):c.5261G>A (p.Arg1754His)	rs544020493	0.00002
NM_016239.4(MYO15A):c.328C>T (p.Arg110Cys)	rs779554298	0.00001
NM_016239.4(MYO15A):c.8644G>A (p.Asp2882Asn)	rs752873001	0.00001
NM_016239.4(MYO15A):c.3358C>T (p.Arg1120Cys)	rs375451997
NM_016239.4(MYO15A):c.458A>G (p.Gln153Arg)	rs1597748342
NM_016239.4(MYO15A):c.6550T>C (p.Cys2184Arg)	rs1567649779
NM_016239.4(MYO15A):c.8590G>C (p.Glu2864Gln)	rs1555546843
NM_016239.4(MYO15A):c.8882C>T (p.Thr2961Met)	rs1347316160
NM_016239.4(MYO15A):c.9785G>C (p.Arg3262Pro)	rs368106470

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