List of variants in gene TTN reported as not provided for cardiomyopathy

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.24820G>A (p.Glu8274Lys)	rs72648981	0.00245
NM_001267550.2(TTN):c.68458G>C (p.Ala22820Pro)	rs72646880	0.00151
NM_133379.5(TTN):c.11075G>C (p.Ser3692Thr)	rs147314430	0.00071
NM_001267550.2(TTN):c.88720C>T (p.Arg29574Cys)	rs200513274	0.00029
NM_001267550.2(TTN):c.106537A>G (p.Lys35513Glu)	rs551063889	0.00006
NM_001267550.2(TTN):c.34930+2T>C	rs749252830	0.00004
NM_001267550.2(TTN):c.9443G>A (p.Arg3148His)	rs368786036	0.00004
NM_001267550.2(TTN):c.49648+2del	rs727504851	0.00003
NM_001267550.2(TTN):c.9610C>T (p.Arg3204Ter)	rs757836789	0.00003
NM_001267550.2(TTN):c.23879G>A (p.Ser7960Asn)	rs369302142	0.00001
NM_001267550.2(TTN):c.44816-1G>A	rs749705939	0.00001
NM_001267550.2(TTN):c.55432+5G>C	rs754717390	0.00001
NM_001267550.2(TTN):c.97050dup (p.Glu32351fs)	rs794729365	0.00001
NM_001267550.2(TTN):c.106201G>A (p.Glu35401Lys)	rs2154132721
NM_001267550.2(TTN):c.107797G>C (p.Gly35933Arg)	rs1575170417
NM_001267550.2(TTN):c.12519_12520del (p.Glu4173fs)	rs1553939605
NM_001267550.2(TTN):c.40558G>C (p.Val13520Leu)	rs587780488
NM_001267550.2(TTN):c.44281+1G>A	rs771562210
NM_001267550.2(TTN):c.51449del (p.Pro17150fs)	rs2055912067
NM_001267550.2(TTN):c.63010G>T (p.Glu21004Ter)	rs769345390
NM_001267550.2(TTN):c.65505del (p.Ile21835fs)	rs1559521007
NM_001267550.2(TTN):c.69051A>G (p.Glu23017=)	rs770296752
NM_001267550.2(TTN):c.72390G>C (p.Leu24130Phe)	rs376664950

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