"Ambry Genetics"[submitter] AND "TDRD1"[gene] - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2518287	NM_001395205.1(TDRD1):c.66G>A (p.Met22Ile)	TDRD1 (M22I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389830	NM_001395205.1(TDRD1):c.134G>A (p.Gly45Glu)	TDRD1 (G45E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365819	NM_001395205.1(TDRD1):c.159C>G (p.Phe53Leu)	TDRD1 (F53L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558235	NM_001395205.1(TDRD1):c.257C>T (p.Ser86Phe)	TDRD1 (S86F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461522	NM_001395205.1(TDRD1):c.266C>T (p.Pro89Leu)	TDRD1 (P89L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238822	NM_001395205.1(TDRD1):c.352G>A (p.Glu118Lys)	TDRD1 (E118K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175432	NM_001395205.1(TDRD1):c.362C>T (p.Ser121Leu)	TDRD1 (S121L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286350	NM_001395205.1(TDRD1):c.371A>G (p.Lys124Arg)	TDRD1 (K124R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469620	NM_001395205.1(TDRD1):c.403C>T (p.Arg135Cys)	TDRD1 (R135C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175433	NM_001395205.1(TDRD1):c.428A>G (p.Asn143Ser)	TDRD1 (N143S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274477	NM_001395205.1(TDRD1):c.464C>T (p.Pro155Leu)	TDRD1 (P155L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239377	NM_001395205.1(TDRD1):c.613G>A (p.Val205Met)	TDRD1 (V205M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268654	NM_001395205.1(TDRD1):c.619A>G (p.Arg207Gly)	TDRD1 (R207G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175435	NM_001395205.1(TDRD1):c.671C>T (p.Thr224Ile)	TDRD1 (T224I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175436	NM_001395205.1(TDRD1):c.802G>T (p.Gly268Cys)	TDRD1 (G268C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349942	NM_001395205.1(TDRD1):c.806C>T (p.Thr269Met)	TDRD1 (T269M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313672	NM_001395205.1(TDRD1):c.907T>A (p.Tyr303Asn)	TDRD1 (Y303N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234489	NM_001395205.1(TDRD1):c.973G>A (p.Val325Ile)	TDRD1 (V325I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387329	NM_001395205.1(TDRD1):c.997A>G (p.Ile333Val)	TDRD1 (I333V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175419	NM_001395205.1(TDRD1):c.1024A>C (p.Lys342Gln)	TDRD1 (K342Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175420	NM_001395205.1(TDRD1):c.1094T>C (p.Leu365Pro)	TDRD1 (L365P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304259	NM_001395205.1(TDRD1):c.1226C>T (p.Ser409Phe)	TDRD1 (S409F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348018	NM_001395205.1(TDRD1):c.1234A>G (p.Ile412Val)	TDRD1 (I412V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517103	NM_001395205.1(TDRD1):c.1288C>A (p.Pro430Thr)	TDRD1 (P430T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175422	NM_001395205.1(TDRD1):c.1309G>A (p.Asp437Asn)	TDRD1 (D389N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530100	NM_001395205.1(TDRD1):c.1313A>G (p.His438Arg)	TDRD1 (H390R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222360	NM_001395205.1(TDRD1):c.1349G>C (p.Ser450Thr)	TDRD1 (S402T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371639	NM_001395205.1(TDRD1):c.1457A>G (p.Lys486Arg)	TDRD1 (K438R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2563454	NM_001395205.1(TDRD1):c.1609C>T (p.Arg537Cys)	TDRD1 (R537C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380746	NM_001395205.1(TDRD1):c.1610G>T (p.Arg537Leu)	TDRD1 (R537L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330870	NM_001395205.1(TDRD1):c.1687G>A (p.Val563Ile)	TDRD1 (V563I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175423	NM_001395205.1(TDRD1):c.1699G>A (p.Ala567Thr)	TDRD1 (A567T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406656	NM_001395205.1(TDRD1):c.1825C>G (p.Leu609Val)	TDRD1 (L561V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175424	NM_001395205.1(TDRD1):c.1834G>A (p.Val612Ile)	TDRD1 (V555I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333205	NM_001395205.1(TDRD1):c.1835T>C (p.Val612Ala)	TDRD1 (V564A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175425	NM_001395205.1(TDRD1):c.1941T>A (p.Ser647Arg)	TDRD1 (S647R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260334	NM_001395205.1(TDRD1):c.1969G>A (p.Glu657Lys)	TDRD1 (E600K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590712	NM_001395205.1(TDRD1):c.1973C>T (p.Thr658Met)	TDRD1 (T610M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175426	NM_001395205.1(TDRD1):c.2084G>A (p.Gly695Asp)	TDRD1 (G638D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344414	NM_001395205.1(TDRD1):c.2152G>A (p.Val718Ile)	TDRD1 (V718I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252020	NM_001395205.1(TDRD1):c.2251G>A (p.Glu751Lys)	TDRD1 (E694K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322689	NM_001395205.1(TDRD1):c.2443T>C (p.Ser815Pro)	TDRD1 (S815P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2399834	NM_001395205.1(TDRD1):c.2498T>C (p.Ile833Thr)	TDRD1 (I833T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229958	NM_001395205.1(TDRD1):c.2623G>A (p.Asp875Asn)	TDRD1 (D827N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175429	NM_001395205.1(TDRD1):c.2702A>G (p.His901Arg)	TDRD1 (H853R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305414	NM_001395205.1(TDRD1):c.2932G>C (p.Glu978Gln)	TDRD1 (E974Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254218	NM_001395205.1(TDRD1):c.2935T>C (p.Tyr979His)	TDRD1 (Y865H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508597	NM_001395205.1(TDRD1):c.2974A>G (p.Arg992Gly)	TDRD1 (R935G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175431	NM_001395205.1(TDRD1):c.2986G>A (p.Ala996Thr)	TDRD1 (A882T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407650	NM_001395205.1(TDRD1):c.3103C>T (p.Leu1035Phe)	TDRD1 (L1031F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467252	NM_001395205.1(TDRD1):c.3254T>A (p.Met1085Lys)	TDRD1 (M1081K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353181	NM_001395205.1(TDRD1):c.3332T>C (p.Val1111Ala)	TDRD1 (V997A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589174	NM_001395205.1(TDRD1):c.3350C>T (p.Thr1117Ile)	TDRD1 (T1060I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523225	NM_001395205.1(TDRD1):c.3370A>G (p.Ile1124Val)	TDRD1 (I1120V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236204	NM_001395205.1(TDRD1):c.3388A>G (p.Ser1130Gly)	TDRD1 (S1016G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362141	NM_001395205.1(TDRD1):c.3389G>A (p.Ser1130Asn)	TDRD1 (S1073N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389382	NM_001395205.1(TDRD1):c.3456A>T (p.Glu1152Asp)	TDRD1 (E1076D +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541603	NM_001395205.1(TDRD1):c.3511T>C (p.Phe1171Leu)	TDRD1 (F1057L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 58