"Ambry Genetics"[submitter] AND "NTRK3-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3202650	NM_001012338.3(NTRK3):c.148G>T (p.Asp50Tyr)	NTRK3, NTRK3-AS1 (D50Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202649	NM_001012338.3(NTRK3):c.140G>A (p.Arg47Gln)	NTRK3-AS1, NTRK3 (R47Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299885	NM_001012338.3(NTRK3):c.137G>C (p.Arg46Pro)	NTRK3, NTRK3-AS1 (R46P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534073	NM_001012338.3(NTRK3):c.131A>G (p.Asn44Ser)	NTRK3, NTRK3-AS1 (N44S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341419	NM_001012338.3(NTRK3):c.83C>T (p.Ser28Phe)	NTRK3, NTRK3-AS1 (S28F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404388	NM_001012338.3(NTRK3):c.41G>A (p.Arg14Gln)	NTRK3, NTRK3-AS1 (R14Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar