"Ambry Genetics"[submitter] AND "TDRD3"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3175460	NM_001146070.2(TDRD3):c.68C>G (p.Ala23Gly)	TDRD3 (A23G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175461	NM_001146070.2(TDRD3):c.82C>T (p.Pro28Ser)	TDRD3 (P28S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3325107	NM_001146070.2(TDRD3):c.94A>G (p.Asn32Asp)	TDRD3 (N32D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227811	NM_001146070.2(TDRD3):c.106A>G (p.Ile36Val)	TDRD3 (I36V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175452	NM_001146070.2(TDRD3):c.155T>C (p.Phe52Ser)	TDRD3 (F52S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3325109	NM_001146070.2(TDRD3):c.250G>A (p.Asp84Asn)	TDRD3 (D84N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175456	NM_001146070.2(TDRD3):c.259G>C (p.Glu87Gln)	TDRD3 (E87Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175457	NM_001146070.2(TDRD3):c.313A>C (p.Ser105Arg)	TDRD3 (S105R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264693	NM_001146070.2(TDRD3):c.385C>T (p.Leu129Phe)	TDRD3 (L129F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368613	NM_001146070.2(TDRD3):c.400G>A (p.Asp134Asn)	TDRD3 (D134N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175458	NM_001146070.2(TDRD3):c.466C>A (p.His156Asn)	TDRD3 (H63N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175459	NM_001146070.2(TDRD3):c.557C>G (p.Pro186Arg)	TDRD3 (P93R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325106	NM_001146070.2(TDRD3):c.801A>T (p.Leu267Phe)	TDRD3 (L174F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595490	NM_001146070.2(TDRD3):c.936T>A (p.Asn312Lys)	TDRD3 (N219K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595335	NM_001146070.2(TDRD3):c.998T>C (p.Met333Thr)	TDRD3 (M333T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175447	NM_001146070.2(TDRD3):c.1033G>A (p.Gly345Arg)	TDRD3 (G252R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175448	NM_001146070.2(TDRD3):c.1055A>G (p.Glu352Gly)	TDRD3 (E259G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175449	NM_001146070.2(TDRD3):c.1073C>A (p.Ala358Glu)	TDRD3 (A358E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175450	NM_001146070.2(TDRD3):c.1244G>A (p.Arg415Gln)	TDRD3 (R322Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325103	NM_001146070.2(TDRD3):c.1258C>A (p.Gln420Lys)	TDRD3 (Q327K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362740	NM_001146070.2(TDRD3):c.1276C>G (p.Pro426Ala)	TDRD3 (P333A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331312	NM_001146070.2(TDRD3):c.1330G>A (p.Gly444Arg)	TDRD3 (G351R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175451	NM_001146070.2(TDRD3):c.1349G>A (p.Gly450Asp)	TDRD3 (G357D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340696	NM_001146070.2(TDRD3):c.1474A>C (p.Ser492Arg)	TDRD3 (S492R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311170	NM_001146070.2(TDRD3):c.1528G>C (p.Gly510Arg)	TDRD3 (G417R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228616	NM_001146070.2(TDRD3):c.1597C>T (p.Arg533Cys)	TDRD3 (R440C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325104	NM_001146070.2(TDRD3):c.1736G>A (p.Arg579Gln)	TDRD3 (R579Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281082	NM_001146070.2(TDRD3):c.1796G>A (p.Arg599Gln)	TDRD3 (R506Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325108	NM_001146070.2(TDRD3):c.1849A>C (p.Lys617Gln)	TDRD3 (K524Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325110	NM_001146070.2(TDRD3):c.1908A>G (p.Ile636Met)	TDRD3 (I636M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325105	NM_001146070.2(TDRD3):c.1915T>A (p.Ser639Thr)	TDRD3 (S639T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292469	NM_001146070.2(TDRD3):c.2090A>G (p.Asn697Ser)	TDRD3 (N697S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175454	NM_001146070.2(TDRD3):c.2138A>G (p.Asp713Gly)	TDRD3 (D620G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386141	NM_001146070.2(TDRD3):c.2156G>A (p.Arg719His)	TDRD3 (R626H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175455	NM_001146070.2(TDRD3):c.2192G>A (p.Arg731Gln)	TDRD3 (R731Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 35