"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC126806424"[gen - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 228116	NM_001267550.2(TTN):c.60198G>A (p.Pro20066=)	LOC126806424, TTN +1 more	Single nucleotide variant (synonymous variant)	not specified +8 more	GBenign/Likely benign
Select item 699534	NM_001267550.2(TTN):c.60195C>A (p.Ile20065=)	LOC126806424, TTN +1 more	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1G +6 more	GLikely benign
Select item 701463	NM_001267550.2(TTN):c.60027C>T (p.Ile20009=)	LOC126806424, TTN +1 more	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 9 +8 more	GLikely benign
Select item 413209	NM_001267550.2(TTN):c.60003G>A (p.Pro20001=)	LOC126806424, TTN +1 more	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +6 more	GLikely benign
Select item 165933	NM_001267550.2(TTN):c.59926C>T (p.His19976Tyr)	LOC126806424, TTN +1 more (H17408Y +5 more)	Single nucleotide variant (missense variant)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 332822	NM_001267550.2(TTN):c.59912C>T (p.Ala19971Val)	LOC126806424, TTN +1 more (A19971V +5 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +10 more	GUncertain significance
Select item 535399	NM_001267550.2(TTN):c.59813C>T (p.Ala19938Val)	LOC126806424, TTN +1 more (A19938V +5 more)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 178203	NM_001267550.2(TTN):c.59729C>T (p.Thr19910Ile)	LOC126806424, TTN +1 more (T17342I +5 more)	Single nucleotide variant (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 535436	NM_001267550.2(TTN):c.59711A>G (p.Asp19904Gly)	TTN-AS1, LOC126806424 +1 more (D19904G +5 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1G +5 more	GUncertain significance
Select item 47154	NM_001267550.2(TTN):c.59707G>A (p.Asp19903Asn)	LOC126806424, TTN +1 more (D19903N +5 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +8 more	GConflicting classifications of pathogenicity
Select item 229476	NM_001267550.2(TTN):c.59570T>C (p.Leu19857Ser)	LOC126806424, TTN +1 more (L17289S +5 more)	Single nucleotide variant (missense variant)	not specified +7 more	GUncertain significance
Select item 405007	NM_001267550.2(TTN):c.59489A>G (p.Lys19830Arg)	LOC126806424, TTN +1 more (K19830R +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GUncertain significance
Select item 467328	NM_001267550.2(TTN):c.59474G>C (p.Arg19825Thr)	LOC126806424, TTN +1 more (R19825T +5 more)	Single nucleotide variant (missense variant)	not specified +7 more	GConflicting classifications of pathogenicity