List of variants in gene MYO3A reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_017433.5(MYO3A):c.1275G>A (p.Gln425=)	rs77562287	0.00150
NM_017433.5(MYO3A):c.424C>T (p.His142Tyr)	rs140301218	0.00121
NM_017433.5(MYO3A):c.1566A>C (p.Gly522=)	rs139121564	0.00111
NM_017433.5(MYO3A):c.1500G>A (p.Ala500=)	rs146797033	0.00104
NM_017433.5(MYO3A):c.585+4A>T	rs202189844	0.00095
NM_017433.5(MYO3A):c.177C>T (p.Asp59=)	rs139958275	0.00085
NM_017433.5(MYO3A):c.2214T>C (p.Asn738=)	rs34803755	0.00084
NM_017433.5(MYO3A):c.3538G>A (p.Glu1180Lys)	rs184043065	0.00078
NM_017433.5(MYO3A):c.546G>T (p.Arg182=)	rs148349532	0.00072
NM_017433.5(MYO3A):c.3729G>A (p.Arg1243=)	rs146832858	0.00069
NM_017433.5(MYO3A):c.3037C>T (p.Arg1013Cys)	rs140154015	0.00049
NM_017433.5(MYO3A):c.3255C>T (p.Ser1085=)	rs35541310	0.00044
NM_017433.5(MYO3A):c.3880A>G (p.Ile1294Val)	rs56261037	0.00041
NM_017433.5(MYO3A):c.3352A>G (p.Thr1118Ala)	rs138955440	0.00037
NM_017433.5(MYO3A):c.3000-11T>C	rs375346333	0.00036
NM_017433.5(MYO3A):c.3932C>G (p.Thr1311Ser)	rs146693681	0.00033
NM_017433.5(MYO3A):c.4045G>C (p.Ala1349Pro)	rs149521185	0.00026
NM_017433.5(MYO3A):c.4073G>A (p.Arg1358Gln)	rs141903506	0.00020
NM_017433.5(MYO3A):c.3730T>C (p.Tyr1244His)	rs148993025	0.00019
NM_017433.5(MYO3A):c.1668A>G (p.Leu556=)	rs112809849	0.00018
NM_017433.5(MYO3A):c.4730+11A>C	rs375717548	0.00017
NM_017433.5(MYO3A):c.906G>A (p.Thr302=)	rs139818474	0.00014
NM_017433.5(MYO3A):c.4846T>C (p.Ser1616Pro)	rs767228097	0.00008
NM_017433.5(MYO3A):c.3027C>T (p.Ser1009=)	rs141341808	0.00007
NM_017433.5(MYO3A):c.542G>A (p.Arg181His)	rs574220416	0.00006
NM_017433.5(MYO3A):c.1725C>G (p.Ser575=)	rs201882363	0.00004
NM_017433.5(MYO3A):c.4350T>C (p.Ile1450=)	rs397517294	0.00004
NM_017433.5(MYO3A):c.472T>C (p.Leu158=)	rs1412624643	0.00003
NM_017433.5(MYO3A):c.288G>A (p.Leu96=)	rs760525102	0.00001
NM_017433.5(MYO3A):c.4847C>T (p.Ser1616Phe)	rs752615488	0.00001
NM_017433.5(MYO3A):c.1029A>G (p.Leu343=)	rs544012938
NM_017433.5(MYO3A):c.1038A>G (p.Leu346=)	rs727505229
NM_017433.5(MYO3A):c.1080G>A (p.Lys360=)	rs397517293
NM_017433.5(MYO3A):c.1643C>A (p.Pro548His)	rs143918373
NM_017433.5(MYO3A):c.2625G>C (p.Leu875=)	rs371741845
NM_017433.5(MYO3A):c.3585G>T (p.Val1195=)	rs372169216
NM_017433.5(MYO3A):c.3842T>G (p.Phe1281Cys)	rs876657529
NM_017433.5(MYO3A):c.4088G>A (p.Arg1363Lys)	rs876657530

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