"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC1268064 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 759272	NM_001267550.2(TTN):c.21459T>C (p.Asn7153=)	LOC126806428, TTN	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2651687	NM_001267550.2(TTN):c.21442G>A (p.Val7148Ile)	LOC126806428, TTN (V5904I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 46684	NM_001267550.2(TTN):c.21404-4A>G	LOC126806428, TTN	Single nucleotide variant (intron variant)	Early-onset myopathy with fatal cardiomyopathy +7 more	GConflicting classifications of pathogenicity
Select item 46682	NM_001267550.2(TTN):c.21173G>A (p.Gly7058Asp)	LOC126806428, TTN (G7058D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +7 more	GConflicting classifications of pathogenicity
Select item 178244	NM_001267550.2(TTN):c.21148C>T (p.Leu7050=)	LOC126806428, TTN	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1G +7 more	GConflicting classifications of pathogenicity
Select item 499085	NM_001267550.2(TTN):c.21103G>A (p.Val7035Ile)	LOC126806428, TTN (V5791I +2 more)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy +1 more	GUncertain significance
Select item 681986	NM_001267550.2(TTN):c.20874G>A (p.Thr6958=)	LOC126806428, TTN	Single nucleotide variant (synonymous variant +1 more)	not provided +6 more	GBenign/Likely benign

ClinVar