List of variants in gene TTN reported by 3billion, Medical Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.107635C>T (p.Gln35879Ter)	rs757082154	0.00001
NM_001267550.2(TTN):c.103360del (p.Glu34454fs)	rs760768093
NM_001267550.2(TTN):c.107153dup (p.Asn35718fs)
NM_001267550.2(TTN):c.29621_29624del (p.Glu9874fs)	rs777924443
NM_001267550.2(TTN):c.3425dup (p.Ile1143fs)
NM_001267550.2(TTN):c.54000G>A (p.Trp18000Ter)	rs72646813
NM_001267550.2(TTN):c.55578G>A (p.Trp18526Ter)
NM_001267550.2(TTN):c.63390_63393del (p.Phe21130fs)
NM_001267550.2(TTN):c.71602C>T (p.Arg23868Ter)	rs397517689
NM_001267550.2(TTN):c.74767dup (p.Asp24923fs)	rs1343078144
NM_001267550.2(TTN):c.79684C>T (p.Arg26562Ter)	rs869025545
NM_001267550.2(TTN):c.89017C>T (p.Arg29673Ter)	rs886038916
NM_001267550.2(TTN):c.95134T>C (p.Cys31712Arg)	rs869320740

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