"Ambry Genetics"[submitter] AND "TCEANC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2391904	NM_001297563.2(TCEANC):c.37C>G (p.Leu13Val)	TCEANC (L43V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2587946	NM_001297563.2(TCEANC):c.314C>T (p.Pro105Leu)	TCEANC (P135L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2454260	NM_001297563.2(TCEANC):c.712C>T (p.His238Tyr)	TCEANC (H238Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2306765	NM_001297563.2(TCEANC):c.746C>G (p.Ser249Cys)	TCEANC (S249C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326190	NM_001297563.2(TCEANC):c.821C>T (p.Thr274Met)	TCEANC (T274M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510069	NM_001297563.2(TCEANC):c.895C>T (p.Arg299Cys)	TCEANC (R329C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar