List of variants in gene combination LOC126806430, TTN reported as likely benign by GeneDx

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_001267550.2(TTN):c.18659G>C (p.Cys6220Ser)	rs191692293	0.00188
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18172C>T (p.Arg6058Cys)	rs189127014	0.00053
NM_001267550.2(TTN):c.18550G>A (p.Ala6184Thr)	rs72648947	0.00046
NM_001267550.2(TTN):c.18745G>A (p.Asp6249Asn)	rs201263441	0.00021
NM_001267550.2(TTN):c.18407G>A (p.Arg6136Gln)	rs117551279	0.00016
NM_001267550.2(TTN):c.18379T>G (p.Cys6127Gly)	rs370812788	0.00011
NM_001267550.2(TTN):c.18295C>T (p.Leu6099Phe)	rs370109572	0.00010
NM_001267550.2(TTN):c.18557C>T (p.Thr6186Met)	rs200359082	0.00010
NM_001267550.2(TTN):c.18663A>C (p.Glu6221Asp)	rs369544339	0.00010
NM_001267550.2(TTN):c.18307+12A>G	rs376899412	0.00009
NM_001267550.2(TTN):c.18470T>C (p.Ile6157Thr)	rs371882162	0.00009
NM_001267550.2(TTN):c.18843A>G (p.Ser6281=)	rs755958191	0.00008
NM_001267550.2(TTN):c.18893T>C (p.Ile6298Thr)	rs375571785	0.00006
NM_001267550.2(TTN):c.18267T>A (p.Asp6089Glu)	rs754848806	0.00005
NM_001267550.2(TTN):c.18684T>C (p.Phe6228=)	rs368427156	0.00005
NM_001267550.2(TTN):c.18778A>C (p.Lys6260Gln)	rs375652574	0.00005
NM_001267550.2(TTN):c.18528T>C (p.Tyr6176=)	rs375408819	0.00004
NM_001267550.2(TTN):c.18655G>A (p.Glu6219Lys)	rs72648948	0.00004
NM_001267550.2(TTN):c.18681G>A (p.Pro6227=)	rs372273496	0.00004
NM_001267550.2(TTN):c.18719G>A (p.Arg6240Gln)	rs761993856	0.00004
NM_001267550.2(TTN):c.18942C>T (p.Thr6314=)	rs572285982	0.00004
NM_001267550.2(TTN):c.18363G>A (p.Gln6121=)	rs375032616	0.00003
NM_001267550.2(TTN):c.18590-14T>G	rs781455893	0.00003
NM_001267550.2(TTN):c.18645C>T (p.Asp6215=)	rs372400829	0.00003
NM_001267550.2(TTN):c.18307+13C>T	rs201930482	0.00002
NM_001267550.2(TTN):c.18542G>A (p.Arg6181Gln)	rs201951252	0.00002
NM_001267550.2(TTN):c.18720A>G (p.Arg6240=)	rs201395913	0.00002
NM_001267550.2(TTN):c.18777C>A (p.Thr6259=)	rs750180579	0.00002
NM_001267550.2(TTN):c.18717T>A (p.Ile6239=)	rs765483284	0.00001
NM_001267550.2(TTN):c.18744C>T (p.Thr6248=)	rs775965000	0.00001
NM_001267550.2(TTN):c.18249T>C (p.Ile6083=)	rs1057522780
NM_001267550.2(TTN):c.18437T>C (p.Ile6146Thr)	rs1578142340
NM_001267550.2(TTN):c.18869-15C>T	rs749315046

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