List of variants in gene MYH11 reported by Blueprint 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.739C>T (p.Arg247Cys)	rs150759461	0.00174
NM_002474.3(MYH11):c.1871G>A (p.Arg624His)	rs201991156	0.00068
NM_002474.3(MYH11):c.3196G>A (p.Asp1066Asn)	rs200315340	0.00061
NM_002474.3(MYH11):c.508G>A (p.Glu170Lys)	rs766315580	0.00006
NM_002474.3(MYH11):c.2496G>C (p.Trp832Cys)	rs369196744	0.00005
NM_002474.3(MYH11):c.2297G>A (p.Ser766Asn)	rs1050298581	0.00001
NM_002474.3(MYH11):c.418G>A (p.Asp140Asn)	rs1085307699	0.00001
NM_002474.3(MYH11):c.1201A>G (p.Ile401Val)	rs1596795086
NM_002474.3(MYH11):c.2135G>A (p.Arg712Gln)	rs267606902
NM_002474.3(MYH11):c.2141G>C (p.Gly714Ala)	rs1555560489
NM_002474.3(MYH11):c.2545C>T (p.Arg849Trp)	rs869025471
NM_002474.3(MYH11):c.3265GAG[2] (p.Glu1091del)	rs1596756439
NM_002474.3(MYH11):c.3397G>T (p.Ala1133Ser)	rs148731225
NM_002474.3(MYH11):c.3707T>C (p.Leu1236Pro)	rs1596738708
NM_002474.3(MYH11):c.3757AAG[3] (p.Lys1256del)	rs730880147
NM_002474.3(MYH11):c.605A>C (p.His202Pro)	rs369194676

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