List of variants in gene MYO6 reported as likely benign by Illumina Laboratory Services, Illumina

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.1722C>T (p.Asp574=)	rs11756446	0.04242
NM_004999.4(MYO6):c.3303C>T (p.Cys1101=)	rs9443199	0.02151
NM_004999.4(MYO6):c.*1962A>G	rs80199115	0.01750
NM_004999.4(MYO6):c.*3546A>G	rs73751758	0.01688
NM_004999.4(MYO6):c.*1469G>T	rs74367845	0.01285
NM_004999.4(MYO6):c.1176A>G (p.Thr392=)	rs2273857	0.01200
NM_004999.4(MYO6):c.*3509G>A	rs78129547	0.00783
NM_004999.4(MYO6):c.*2910T>A	rs140495245	0.00749
NM_004999.4(MYO6):c.1120T>C (p.Tyr374His)	rs61732664	0.00738
NM_004999.4(MYO6):c.*3288T>C	rs118121148	0.00533
NM_004999.4(MYO6):c.1224-4A>G	rs144031818	0.00238
NM_004999.4(MYO6):c.*4095G>A	rs185154265	0.00151
NM_004999.4(MYO6):c.2517T>C (p.Gly839=)	rs112597191	0.00135
NM_004999.4(MYO6):c.1144G>A (p.Asp382Asn)	rs111530469	0.00134
NM_004999.4(MYO6):c.*303A>G	rs146133231	0.00128
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val)	rs145564837	0.00128
NM_004999.4(MYO6):c.*1232C>T	rs182487428	0.00051
NM_004999.4(MYO6):c.2836C>T (p.Arg946Cys)	rs141845119	0.00039
NM_004999.4(MYO6):c.*3230T>C	rs562815854	0.00038
NM_004999.4(MYO6):c.*3874G>A	rs187631847	0.00032
NM_004999.4(MYO6):c.*4288G>A	rs570588843	0.00029
NM_004999.4(MYO6):c.*1738A>G	rs193019967	0.00028
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys)	rs201507590	0.00026
NM_004999.4(MYO6):c.*4428A>G	rs574549669	0.00024
NM_004999.4(MYO6):c.3483G>A (p.Glu1161=)	rs139174622	0.00024
NM_004999.4(MYO6):c.3176G>C (p.Arg1059Thr)	rs202214380	0.00020
NM_004999.4(MYO6):c.*1889A>G	rs189155544	0.00018
NM_004999.4(MYO6):c.1180G>A (p.Val394Ile)	rs373519764	0.00006
NM_004999.4(MYO6):c.2672C>T (p.Thr891Met)	rs146682372	0.00006
NM_004999.4(MYO6):c.553+10A>G	rs188959117	0.00005
NM_004999.4(MYO6):c.189T>G (p.Cys63Trp)	rs768643110	0.00002
NM_004999.4(MYO6):c.*1139del	rs3834289
NM_004999.4(MYO6):c.*1528C>T	rs188719640
NM_004999.4(MYO6):c.*186A>G	rs571307356
NM_004999.4(MYO6):c.*3039A>G	rs540365866
NM_004999.4(MYO6):c.*3301del	rs199966180
NM_004999.4(MYO6):c.*4113dup	rs138193115
NM_004999.4(MYO6):c.*4283A>T	rs7746476
NM_004999.4(MYO6):c.*4423AATT[1]	rs10547766
NM_004999.4(MYO6):c.*4495AAAT[4]	rs574841371
NM_004999.4(MYO6):c.1078+19dup	rs144408691
NM_004999.4(MYO6):c.1546+7_1546+8del	rs3831003

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