ClinVar Miner

List of variants reported as benign for autosomal dominant distal myopathy by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (33):

Amyotrophic lateral sclerosis type 21
Autosomal dominant nonsyndromic hearing loss 4A; Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy
Cardiomyopathy, familial restrictive, 1; Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement
Dilated cardiomyopathy 1C; Myofibrillar myopathy 4
Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9
Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9
Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Hypertrophic cardiomyopathy 9
Dilated cardiomyopathy 1G; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9
Dilated cardiomyopathy 1G; Myopathy, myofibrillar, 9, with early respiratory failure; Hypertrophic cardiomyopathy 9
Dilated cardiomyopathy 1G; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Hypertrophic cardiomyopathy 9
Distal myopathy with posterior leg and anterior hand involvement
Distal myopathy, Tateyama type
Elevated circulating creatine kinase concentration; Hypertrophic cardiomyopathy 1; Long QT syndrome 9; Rippling muscle disease 2; Distal myopathy, Tateyama type
Finnish upper limb-onset distal myopathy
Myofibrillar myopathy 2
Myofibrillar myopathy 2; Cataract 16 multiple types; Fatal infantile hypertonic myofibrillar myopathy; Dilated cardiomyopathy 1II
Myofibrillar myopathy 3
Myofibrillar myopathy 4
Myofibrillar myopathy 5; Desmin-related myofibrillar myopathy; Distal myopathy with posterior leg and anterior hand involvement; Hypertrophic cardiomyopathy 26
Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement
Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement; Hypertrophic cardiomyopathy 26
Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement; Hypertrophic cardiomyopathy 26; Dilated Cardiomyopathy, Dominant
Myofibrillar myopathy 5; Primary familial hypertrophic cardiomyopathy; Distal myopathy with posterior leg and anterior hand involvement
Myopathy, myofibrillar, 9, with early respiratory failure
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
Primary dilated cardiomyopathy; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy
Primary dilated cardiomyopathy; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure
Primary dilated cardiomyopathy; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Autosomal recessive centronuclear myopathy
Primary dilated cardiomyopathy; Myopathy, centronuclear, 2; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure
Rippling muscle disease 2; Distal myopathy, Tateyama type
Tibial muscular dystrophy
Welander distal myopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.8902+14del	rs573000455	0.16798
NM_001267550.2(TTN):c.8902+16del	rs570467105	0.16737
NM_001267550.2(TTN):c.49648+16T>C	rs57677875	0.01831
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg)	rs34423165	0.01671
NM_001267550.2(TTN):c.4246C>T (p.Arg1416Cys)	rs72647875	0.01559
NM_001267550.2(TTN):c.106476T>C (p.Cys35492=)	rs6725673	0.01548
NM_001267550.2(TTN):c.65516C>T (p.Ala21839Val)	rs55948748	0.01336
NM_001267550.2(TTN):c.104576G>A (p.Arg34859Gln)	rs68080670	0.01276
NM_001458.5(FLNC):c.2390-14C>T	rs71581921	0.00843
NM_001267550.2(TTN):c.49443A>C (p.Pro16481=)	rs74321406	0.00774
NM_001267550.2(TTN):c.14984C>G (p.Pro4995Arg)	rs72648927	0.00729
NM_001267550.2(TTN):c.95035G>A (p.Asp31679Asn)	rs116567963	0.00481
NM_007078.3(LDB3):c.352G>A (p.Val118Met)	rs35507268	0.00408
NM_007078.3(LDB3):c.163G>A (p.Val55Ile)	rs3740343	0.00292
NM_001145809.2(MYH14):c.1329+15C>T	rs200176028	0.00227
NM_001267550.2(TTN):c.6041C>T (p.Thr2014Ile)	rs189149543	0.00070
NM_001267550.2(TTN):c.87877C>T (p.Arg29293Cys)	rs191482653	0.00057
NM_001458.5(FLNC):c.7614G>T (p.Leu2538Phe)	rs180834558	0.00041
NM_001458.5(FLNC):c.3964+9C>T	rs200448727	0.00033
NM_001267550.2(TTN):c.82692G>A (p.Ala27564=)	rs557628408	0.00004
NM_001267550.2(TTN):c.39085C>A (p.Pro13029Thr)	rs397517553	0.00002
NM_001267550.2(TTN):c.67637-9A>G	rs2047164551	0.00001
NM_001267550.2(TTN):c.12780G>A (p.Ala4260=)	rs746578
NM_001267550.2(TTN):c.12780G>T (p.Ala4260=)	rs746578
NM_001267550.2(TTN):c.82385C>A (p.Thr27462Lys)	rs55933739

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.