List of variants in gene TTN reported by GeneReviews

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.102271C>T (p.Arg34091Trp)	rs140319117	0.00095
NM_001267550.2(TTN):c.95195C>T (p.Pro31732Leu)	rs753334568	0.00001
NM_001267550.2(TTN):c.107647del (p.Ser35883fs)	rs281864932
NM_001267550.2(TTN):c.107780_107790delinsTGAAAGAAAAA (p.Glu35927_Trp35930delinsValLysGluLys)	rs281864927
NM_001267550.2(TTN):c.107837A>C (p.His35946Pro)	rs281864931
NM_001267550.2(TTN):c.107840T>A (p.Ile35947Asn)	rs281864928
NM_001267550.2(TTN):c.107867T>C (p.Leu35956Pro)	rs267607156
NM_001267550.2(TTN):c.107889del (p.Lys35963fs)	rs281864930
NM_001267550.2(TTN):c.107890C>T (p.Gln35964Ter)	rs281864929
NM_001267550.2(TTN):c.107892_107897del (p.Gln35964_Gly35966delinsHis)	rs281864933
NM_001267550.2(TTN):c.95126C>G (p.Pro31709Arg)	rs869320739
NM_001267550.2(TTN):c.95134T>C (p.Cys31712Arg)	rs869320740
NM_001267550.2(TTN):c.95185T>C (p.Trp31729Arg)	rs869320741
NM_001267550.2(TTN):c.95186G>T (p.Trp31729Leu)	rs786205367
NM_001267550.2(TTN):c.95187G>C (p.Trp31729Cys)	rs869320742
NM_001267550.2(TTN):c.95358C>G (p.Asn31786Lys)	rs869320743
TTN:c.106668delA (p.Lys35556Argfs)	rs587776772

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