"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRDN"[gen - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259915	NM_006073.4(TRDN):c.2051-19G>A	TRDN	Single nucleotide variant (intron variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GBenign
Select item 463675	NM_006073.4(TRDN):c.1975+9G>A	TRDN	Single nucleotide variant (intron variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GBenign/Likely benign
Select item 936718	NM_006073.4(TRDN):c.1952-5T>C	TRDN	Single nucleotide variant (intron variant)	TRDN-related disorder +1 more	GLikely benign
Select item 3036990	NM_006073.4(TRDN):c.1952-8C>G	TRDN	Single nucleotide variant (intron variant)	TRDN-related disorder	GLikely benign
Select item 699267	NM_006073.4(TRDN):c.1832-4C>A	TRDN	Single nucleotide variant (intron variant)	not provided +3 more	GLikely benign
Select item 3036578	NM_006073.4(TRDN):c.1805-6del	TRDN	Deletion (intron variant)	TRDN-related disorder	GLikely benign
Select item 1164136	NM_006073.4(TRDN):c.1805-6C>T	TRDN	Single nucleotide variant (intron variant)	TRDN-related disorder +2 more	GBenign/Likely benign
Select item 227115	NM_006073.4(TRDN):c.1620A>G (p.Ile540Met)	TRDN (I540M)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GBenign/Likely benign
Select item 227114	NM_006073.4(TRDN):c.1598-6dup	TRDN	Duplication	not specified +3 more	GBenign/Likely benign
Select item 415181	NM_006073.4(TRDN):c.1510G>A (p.Gly504Ser)	TRDN (G504S)	Single nucleotide variant (missense variant)	TRDN-related disorder +4 more	GLikely benign
Select item 227112	NM_006073.4(TRDN):c.1408C>A (p.Leu470Met)	TRDN (L470M)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 227111	NM_006073.4(TRDN):c.1370-11C>A	TRDN	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 227110	NM_006073.4(TRDN):c.1313T>G (p.Ile438Ser)	TRDN (I438S +1 more)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 5 +3 more	GBenign
Select item 227109	NM_006073.4(TRDN):c.1313T>A (p.Ile438Asn)	TRDN (I438N +1 more)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 5 +4 more	GBenign/Likely benign
Select item 227108	NM_006073.4(TRDN):c.1257C>A (p.Asp419Glu)	TRDN (D419E +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 227107	NM_006073.4(TRDN):c.1211T>G (p.Val404Gly)	TRDN (V404G +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GBenign/Likely benign
Select item 227106	NM_006073.4(TRDN):c.1188A>G (p.Lys396=)	TRDN	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GBenign
Select item 561136	NM_006073.4(TRDN):c.1187-2A>G	TRDN	Single nucleotide variant (splice acceptor variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 259914	NM_006073.4(TRDN):c.1186+16C>T	TRDN	Single nucleotide variant (intron variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GBenign
Select item 227105	NM_006073.4(TRDN):c.1105+5G>A	TRDN	Single nucleotide variant (intron variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GBenign
Select item 227104	NM_006073.4(TRDN):c.1096G>A (p.Ala366Thr)	TRDN (A366T +1 more)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 5 +3 more	GBenign/Likely benign
Select item 227102	NM_006073.4(TRDN):c.1016G>A (p.Ser339Asn)	TRDN (S339N +1 more)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GBenign/Likely benign
Select item 1571569	NM_006073.4(TRDN):c.854-7T>C	TRDN-AS1, TRDN	Single nucleotide variant (intron variant)	TRDN-related disorder +1 more	GLikely benign
Select item 3057440	NM_006073.4(TRDN):c.793+29A>T	TRDN	Single nucleotide variant (synonymous variant +1 more)	TRDN-related disorder	GLikely benign
Select item 504836	NM_006073.4(TRDN):c.793+27G>A	TRDN (G274R)	Single nucleotide variant (missense variant +1 more)	TRDN-related disorder +2 more	GLikely benign
Select item 227123	NM_006073.4(TRDN):c.601C>G (p.Leu201Val)	TRDN (L201V)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GBenign
Select item 227122	NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1])	TRDN	Microsatellite (inframe_deletion)	Catecholaminergic polymorphic ventricular tachycardia 5 +4 more	GBenign
Select item 240287	NM_006073.4(TRDN):c.502G>A (p.Glu168Lys)	TRDN (E168K)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 5 +3 more	GLikely benign
Select item 3052551	NM_006073.4(TRDN):c.484+1229T>C	TRDN	Single nucleotide variant (synonymous variant +1 more)	TRDN-related disorder	GLikely benign
Select item 2635811	NM_006073.4(TRDN):c.484+1189G>A	TRDN	Single nucleotide variant (intron variant)	TRDN-related disorder	GLikely pathogenic
Select item 227121	NM_006073.4(TRDN):c.430C>T (p.His144Tyr)	TRDN (H144Y)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GBenign/Likely benign
Select item 227119	NM_006073.4(TRDN):c.383C>G (p.Thr128Ser)	TRDN (T128S)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 2634568	NM_006073.4(TRDN):c.326del (p.Leu109fs)	TRDN (L109fs)	Deletion (frameshift variant)	TRDN-related disorder	GLikely pathogenic
Select item 449704	NM_006073.4(TRDN):c.239C>T (p.Ser80Phe)	TRDN (S80F)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GConflicting classifications of pathogenicity
Select item 355230	NM_006073.4(TRDN):c.-26A>G	TRDN	Single nucleotide variant (5 prime UTR variant)	TRDN-related disorder +1 more	GLikely benign

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Items: 35