"PreventionGenetics, part of Exact Sciences"[submitter] AND "NTRK3"[ge - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050423	NM_001012338.3(NTRK3):c.1933C>T (p.Arg645Cys)	NTRK3 (R547C +2 more)	Single nucleotide variant (missense variant)	NTRK3-related disorder	GBenign
Select item 736201	NM_001012338.3(NTRK3):c.1896T>C (p.His632=)	NTRK3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3059099	NM_001012338.3(NTRK3):c.1767C>T (p.Ala589=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GBenign
Select item 725325	NM_001012338.3(NTRK3):c.1704T>C (p.Leu568=)	NTRK3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3039281	NM_001012338.3(NTRK3):c.1686G>A (p.Pro562=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GLikely benign
Select item 719516	NM_001012338.3(NTRK3):c.1665C>T (p.Ala555=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder +1 more	GBenign/Likely benign
Select item 784618	NM_001012338.3(NTRK3):c.1503G>A (p.Val501=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder +1 more	GBenign
Select item 1251369	NM_001012338.3(NTRK3):c.1488C>G (p.Ala496=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder +1 more	GBenign
Select item 3055801	NM_001012338.3(NTRK3):c.1458C>T (p.His486=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GBenign
Select item 3033741	NM_001012338.3(NTRK3):c.1173C>T (p.Ile391=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GLikely benign
Select item 3046594	NM_001012338.3(NTRK3):c.1035C>G (p.Ser345=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GLikely benign
Select item 3035627	NM_001012338.3(NTRK3):c.930G>T (p.Leu310=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GLikely benign
Select item 791596	NM_001012338.3(NTRK3):c.802T>C (p.Leu268=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder +1 more	GBenign/Likely benign
Select item 3053276	NM_001012338.3(NTRK3):c.516G>A (p.Gln172=)	NTRK3	Single nucleotide variant (synonymous variant)	NTRK3-related disorder	GLikely benign
Select item 719029	NM_001012338.3(NTRK3):c.61G>T (p.Val21Phe)	NTRK3, NTRK3-AS1 (V21F)	Single nucleotide variant (missense variant)	NTRK3-related disorder +1 more	GLikely benign
Select item 3041033	NM_001012338.3(NTRK3):c.-1G>A	NTRK3, NTRK3-AS1	Single nucleotide variant (5 prime UTR variant)	NTRK3-related disorder	GLikely benign