"Ambry Genetics"[submitter] AND "LOC129997046"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3136735	NM_001010919.3(CALHM6):c.457G>C (p.Val153Leu)	CALHM6, CALHM6-AS1 +1 more (V153L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136737	NM_001010919.3(CALHM6):c.461C>T (p.Pro154Leu)	CALHM6, CALHM6-AS1 +1 more (P154L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136736	NM_001010919.3(CALHM6):c.461C>G (p.Pro154Arg)	CALHM6, CALHM6-AS1 +1 more (P154R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527507	NM_001010919.3(CALHM6):c.464G>A (p.Cys155Tyr)	CALHM6, CALHM6-AS1 +1 more (C155Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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