List of variants in gene TTN reported as likely benign by Molecular Genetics, Royal Melbourne Hospital

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.101212C>T (p.Arg33738Cys)	rs56273463	0.00613
NM_001267550.2(TTN):c.72132T>C (p.Gly24044=)	rs56169243	0.00400
NM_001267550.2(TTN):c.69130C>T (p.Pro23044Ser)	rs55980498	0.00372
NM_001267550.2(TTN):c.10114+5G>A	rs115985443	0.00334
NM_001267550.2(TTN):c.67099T>C (p.Ser22367Pro)	rs72646873	0.00195
NM_001267550.2(TTN):c.92176C>T (p.Pro30726Ser)	rs72648247	0.00184
NM_001267550.2(TTN):c.87412C>A (p.Pro29138Thr)	rs72648227	0.00073
NM_001267550.2(TTN):c.15178G>C (p.Val5060Leu)	rs72648929
NM_001267550.2(TTN):c.5993G>A (p.Arg1998His)	rs144135510

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