"PreventionGenetics, part of Exact Sciences"[submitter] AND "TTC19"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3037618	NM_017775.3(TTC19):c.-50G>T	LOC130060311, TTC19	Single nucleotide variant	TTC19-related condition	GLikely benign
Select item 215298	NM_017775.3(TTC19):c.-44A>G	LOC130060311, TTC19	Single nucleotide variant	not specified +1 more	GLikely benign
Select item 321941	NM_017775.4(TTC19):c.146C>T (p.Pro49Leu)	LOC130060311, TTC19 (P49L)	Single nucleotide variant (5 prime UTR variant +1 more)	Mitochondrial complex III deficiency nuclear type 2 +2 more	GConflicting classifications of pathogenicity
Select item 3035375	NM_017775.4(TTC19):c.273G>A (p.Glu91=)	TTC19	Single nucleotide variant (5 prime UTR variant +1 more)	TTC19-related condition	GLikely benign
Select item 215304	NM_017775.4(TTC19):c.820A>G (p.Arg274Gly)	TTC19 (R274G +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 725634	NM_017775.4(TTC19):c.865C>T (p.Leu289=)	TTC19	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 749241	NM_017775.4(TTC19):c.898A>C (p.Ile300Leu)	TTC19 (I300L +1 more)	Single nucleotide variant (missense variant)	TTC19-related condition +2 more	GConflicting classifications of pathogenicity
Select item 215296	NM_017775.4(TTC19):c.911G>C (p.Arg304Thr)	TTC19 (R304T +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 215297	NM_017775.4(TTC19):c.1004C>T (p.Thr335Ile)	TTC19 (T335I +1 more)	Single nucleotide variant (missense variant)	TTC19-related condition +3 more	GConflicting classifications of pathogenicity
Select item 726341	NM_006311.4(NCOR1):c.7074A>G (p.Ser2358=)	NCOR1, TTC19	Single nucleotide variant (synonymous variant)	NCOR1-related condition +1 more	GBenign/Likely benign
Select item 722211	NM_006311.4(NCOR1):c.6870G>A (p.Met2290Ile)	NCOR1, TTC19 (M2290I +1 more)	Single nucleotide variant (missense variant)	NCOR1-related condition +1 more	GBenign/Likely benign
Select item 2633641	NM_006311.4(NCOR1):c.6728C>T (p.Thr2243Met)	NCOR1, TTC19 (T2140M +1 more)	Single nucleotide variant (missense variant)	NCOR1-related condition	GUncertain significance