List of variants in gene MYH11 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 34

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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.3604G>A (p.Ala1202Thr)	rs112657320	0.00093
NM_002474.3(MYH11):c.2005C>T (p.Arg669Cys)	rs111404182	0.00079
NM_002474.3(MYH11):c.472G>A (p.Ala158Thr)	rs375998236	0.00034
NM_002474.3(MYH11):c.2648C>T (p.Ser883Leu)	rs35035518	0.00031
NM_002474.3(MYH11):c.2893G>T (p.Ala965Ser)	rs113696032	0.00031
NM_002474.3(MYH11):c.1502G>A (p.Arg501His)	rs144244239	0.00029
NM_002474.3(MYH11):c.2075C>T (p.Ala692Val)	rs148893135	0.00028
NM_002474.3(MYH11):c.1078G>A (p.Val360Ile)	rs111677442	0.00021
NM_002474.3(MYH11):c.3291C>T (p.Ala1097=)	rs147605116	0.00016
NM_002474.3(MYH11):c.3562C>T (p.Arg1188Trp)	rs146388001	0.00011
NM_002474.3(MYH11):c.405G>A (p.Ser135=)	rs375649016	0.00011
NM_002474.3(MYH11):c.3204C>T (p.His1068=)	rs140143700	0.00009
NM_002474.3(MYH11):c.1344T>C (p.His448=)	rs549593465	0.00008
NM_002474.3(MYH11):c.1913C>T (p.Ser638Leu)	rs771128441	0.00006
NM_002474.3(MYH11):c.1864+19G>A	rs200979632	0.00004
NM_002474.3(MYH11):c.3396C>T (p.Ala1132=)	rs753096245	0.00004
NM_002474.3(MYH11):c.2442C>T (p.Thr814=)	rs759602174	0.00003
NM_002474.3(MYH11):c.3104T>C (p.Met1035Thr)	rs557463209	0.00003
NM_002474.3(MYH11):c.1130-13T>C	rs752403056	0.00002
NM_002474.3(MYH11):c.1879G>A (p.Gly627Ser)	rs563865467	0.00002
NM_002474.3(MYH11):c.1823A>G (p.Asn608Ser)	rs750642581	0.00001
NM_002474.3(MYH11):c.1852C>T (p.Leu618=)	rs759239390	0.00001
NM_002474.3(MYH11):c.3469G>A (p.Asp1157Asn)	rs746943696	0.00001
NM_002474.3(MYH11):c.3594G>A (p.Arg1198=)	rs138908402	0.00001
NM_002474.3(MYH11):c.573C>T (p.Val191=)	rs763981310	0.00001
NM_002474.3(MYH11):c.1074T>C (p.Asn358=)	rs2151282590
NM_002474.3(MYH11):c.1707C>G (p.Leu569=)
NM_002474.3(MYH11):c.1764G>C (p.Ala588=)	rs375133214
NM_002474.3(MYH11):c.1791C>T (p.Asp597=)	rs1305382714
NM_002474.3(MYH11):c.1929C>T (p.Ser643=)	rs1456500560
NM_002474.3(MYH11):c.2055G>A (p.Lys685=)	rs909578082
NM_002474.3(MYH11):c.3198C>T (p.Asp1066=)	rs757270167
NM_002474.3(MYH11):c.555C>T (p.Thr185=)	rs1266756941

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