List of variants in gene LOC126806427, TTN studied for Dilated cardiomyopathy 1G

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.45526C>T (p.Leu15176=)	rs61004744	0.02387
NM_001267550.2(TTN):c.45206A>T (p.Glu15069Val)	rs114331773	0.01832
NM_001267550.2(TTN):c.45328G>A (p.Asp15110Asn)	rs17354992	0.00698
NM_001267550.2(TTN):c.45083-10A>G	rs72677222	0.00683
NM_001267550.2(TTN):c.45350-13T>C	rs113084617	0.00600
NM_001267550.2(TTN):c.45408G>T (p.Lys15136Asn)	rs72677225	0.00512
NM_001267550.2(TTN):c.45175G>A (p.Ala15059Thr)	rs144668626	0.00104
NM_001267550.2(TTN):c.45599C>G (p.Ala15200Gly)	rs201057307	0.00033
NM_001267550.2(TTN):c.45273C>T (p.Asn15091=)	rs72677223	0.00028
NM_001267550.2(TTN):c.45054G>A (p.Ala15018=)	rs781392140	0.00004
NM_001267550.2(TTN):c.45212T>C (p.Ile15071Thr)	rs184078045	0.00004
NM_001267550.2(TTN):c.45322C>T (p.Arg15108Ter)	rs1060500405	0.00001
NM_001267550.2(TTN):c.44999T>C (p.Ile15000Thr)	rs886055275
NM_001267550.2(TTN):c.45120T>G (p.Ile15040Met)	rs74580375
NM_001267550.2(TTN):c.45567C>G (p.Tyr15189Ter)

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