ClinVar for Gene (Select 221400) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3357443	NM_001010870.3(TDRD6):c.484C>T (p.Gln162Ter)	TDRD6 (Q162*)	Single nucleotide variant (nonsense)	TDRD6-related disorder	GLikely benign
Select item 3344102	NM_001010870.3(TDRD6):c.254G>A (p.Arg85His)	TDRD6 (R85H)	Single nucleotide variant (missense variant)	TDRD6-related disorder	GUncertain significance
Select item 3325145	NM_001010870.3(TDRD6):c.146A>G (p.Glu49Gly)	TDRD6 (E49G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325143	NM_001010870.3(TDRD6):c.3155G>C (p.Gly1052Ala)	TDRD6 (G1052A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325142	NM_001010870.3(TDRD6):c.1232T>C (p.Phe411Ser)	TDRD6 (F411S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325141	NM_001010870.3(TDRD6):c.266G>A (p.Arg89Gln)	TDRD6 (R89Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325140	NM_001010870.3(TDRD6):c.5872C>T (p.His1958Tyr)	TDRD6 (H1958Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325139	NM_001010870.3(TDRD6):c.1811A>G (p.Asp604Gly)	TDRD6 (D604G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325138	NM_001010870.3(TDRD6):c.3802A>C (p.Lys1268Gln)	TDRD6 (K1268Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325137	NM_001010870.3(TDRD6):c.760G>T (p.Val254Leu)	TDRD6 (V254L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325136	NM_001010870.3(TDRD6):c.6209A>C (p.Asn2070Thr)	TDRD6 (N2070T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3325135	NM_001010870.3(TDRD6):c.1924G>A (p.Val642Ile)	TDRD6 (V642I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325134	NM_001010870.3(TDRD6):c.3716A>G (p.Tyr1239Cys)	TDRD6 (Y1239C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325133	NM_001010870.3(TDRD6):c.1648A>G (p.Asn550Asp)	TDRD6 (N550D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325132	NM_001010870.3(TDRD6):c.4321C>T (p.Arg1441Trp)	TDRD6 (R1441W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325131	NM_001010870.3(TDRD6):c.3560T>G (p.Met1187Arg)	TDRD6 (M1187R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325130	NM_001010870.3(TDRD6):c.2825C>G (p.Thr942Ser)	TDRD6 (T942S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325129	NM_001010870.3(TDRD6):c.3328G>A (p.Glu1110Lys)	TDRD6 (E1110K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325128	NM_001010870.3(TDRD6):c.5008A>G (p.Ile1670Val)	TDRD6 (I1670V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325127	NM_001010870.3(TDRD6):c.4603T>C (p.Trp1535Arg)	TDRD6 (W1535R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325126	NM_001010870.3(TDRD6):c.5524G>A (p.Asp1842Asn)	TDRD6 (D1842N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325125	NM_001010870.3(TDRD6):c.4405A>G (p.Ile1469Val)	TDRD6 (I1469V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325124	NM_001010870.3(TDRD6):c.4394A>C (p.Glu1465Ala)	TDRD6 (E1465A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325123	NM_001010870.3(TDRD6):c.2657A>G (p.Asn886Ser)	TDRD6 (N886S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325122	NM_001010870.3(TDRD6):c.6035A>G (p.Asp2012Gly)	TDRD6 (D2012G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325121	NM_001010870.3(TDRD6):c.4069G>T (p.Asp1357Tyr)	TDRD6 (D1357Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325120	NM_001010870.3(TDRD6):c.3844G>A (p.Gly1282Arg)	TDRD6 (G1282R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325119	NM_001010870.3(TDRD6):c.2643G>C (p.Arg881Ser)	TDRD6 (R881S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325118	NM_001010870.3(TDRD6):c.1924G>C (p.Val642Leu)	TDRD6 (V642L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325117	NM_001010870.3(TDRD6):c.3398C>T (p.Pro1133Leu)	TDRD6 (P1133L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175517	NM_001010870.3(TDRD6):c.92A>C (p.Gln31Pro)	TDRD6 (Q31P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175516	NM_001010870.3(TDRD6):c.862C>T (p.Arg288Trp)	TDRD6 (R288W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175515	NM_001010870.3(TDRD6):c.770C>G (p.Thr257Ser)	TDRD6 (T257S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175514	NM_001010870.3(TDRD6):c.685C>G (p.Arg229Gly)	TDRD6 (R229G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175513	NM_001010870.3(TDRD6):c.6088G>A (p.Gly2030Arg)	TDRD6 (G2030R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175512	NM_001010870.3(TDRD6):c.5706G>T (p.Glu1902Asp)	TDRD6 (E1902D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175511	NM_001010870.3(TDRD6):c.5675C>T (p.Thr1892Ile)	TDRD6 (T1892I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175510	NM_001010870.3(TDRD6):c.5633T>C (p.Leu1878Pro)	TDRD6 (L1878P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175509	NM_001010870.3(TDRD6):c.5506G>A (p.Glu1836Lys)	TDRD6 (E1836K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175507	NM_001010870.3(TDRD6):c.5098A>G (p.Lys1700Glu)	TDRD6 (K1700E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175506	NM_001010870.3(TDRD6):c.5010C>G (p.Ile1670Met)	TDRD6 (I1670M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175505	NM_001010870.3(TDRD6):c.4964A>G (p.Tyr1655Cys)	TDRD6 (Y1655C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175504	NM_001010870.3(TDRD6):c.476G>A (p.Ser159Asn)	TDRD6 (S159N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175503	NM_001010870.3(TDRD6):c.4753T>C (p.Tyr1585His)	TDRD6 (Y1585H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175502	NM_001010870.3(TDRD6):c.4736G>C (p.Arg1579Thr)	TDRD6 (R1579T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175501	NM_001010870.3(TDRD6):c.4290T>G (p.Asn1430Lys)	TDRD6 (N1430K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175500	NM_001010870.3(TDRD6):c.4262A>G (p.Gln1421Arg)	TDRD6 (Q1421R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175499	NM_001010870.3(TDRD6):c.4135C>T (p.Pro1379Ser)	TDRD6 (P1379S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175498	NM_001010870.3(TDRD6):c.4111C>T (p.Arg1371Cys)	TDRD6 (R1371C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175497	NM_001010870.3(TDRD6):c.410C>A (p.Ala137Glu)	TDRD6 (A137E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175496	NM_001010870.3(TDRD6):c.4054C>T (p.Pro1352Ser)	TDRD6 (P1352S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175495	NM_001010870.3(TDRD6):c.3967C>G (p.Gln1323Glu)	TDRD6 (Q1323E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175494	NM_001010870.3(TDRD6):c.3841A>G (p.Ile1281Val)	TDRD6 (I1281V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175493	NM_001010870.3(TDRD6):c.3689T>C (p.Leu1230Ser)	TDRD6 (L1230S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175492	NM_001010870.3(TDRD6):c.3401A>G (p.Asp1134Gly)	TDRD6 (D1134G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175491	NM_001010870.3(TDRD6):c.3308T>C (p.Ile1103Thr)	TDRD6 (I1103T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175490	NM_001010870.3(TDRD6):c.3249T>G (p.Ser1083Arg)	TDRD6 (S1083R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175489	NM_001010870.3(TDRD6):c.2930A>G (p.Tyr977Cys)	TDRD6 (Y977C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175488	NM_001010870.3(TDRD6):c.243G>T (p.Trp81Cys)	TDRD6 (W81C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175487	NM_001010870.3(TDRD6):c.2423A>G (p.Tyr808Cys)	TDRD6 (Y808C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175486	NM_001010870.3(TDRD6):c.2285C>T (p.Ser762Phe)	TDRD6 (S762F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175485	NM_001010870.3(TDRD6):c.1868C>G (p.Thr623Ser)	TDRD6 (T623S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175484	NM_001010870.3(TDRD6):c.1849G>A (p.Val617Ile)	TDRD6 (V617I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175483	NM_001010870.3(TDRD6):c.1668A>G (p.Ile556Met)	TDRD6 (I556M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175482	NM_001010870.3(TDRD6):c.1529A>G (p.Asn510Ser)	TDRD6 (N510S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175481	NM_001010870.3(TDRD6):c.1217A>G (p.Asn406Ser)	TDRD6 (N406S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175480	NM_001010870.3(TDRD6):c.1165T>C (p.Ser389Pro)	TDRD6 (S389P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175479	NM_001010870.3(TDRD6):c.1159G>A (p.Gly387Ser)	TDRD6 (G387S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3054214	NM_001010870.3(TDRD6):c.1319G>A (p.Cys440Tyr)	TDRD6 (C440Y)	Single nucleotide variant (missense variant)	TDRD6-related disorder	GLikely benign
Select item 3053361	NM_001010870.3(TDRD6):c.1592A>G (p.Asp531Gly)	TDRD6 (D531G)	Single nucleotide variant (missense variant)	TDRD6-related disorder	GLikely benign
Select item 3050329	NM_001010870.3(TDRD6):c.1857T>G (p.Phe619Leu)	TDRD6 (F619L)	Single nucleotide variant (missense variant)	TDRD6-related disorder	GLikely benign
Select item 3037119	NM_001010870.3(TDRD6):c.5865G>A (p.Met1955Ile)	TDRD6 (M1955I)	Single nucleotide variant (missense variant)	TDRD6-related disorder	GLikely benign
Select item 2656631	NM_001010870.3(TDRD6):c.5623A>G (p.Asn1875Asp)	TDRD6 (N1875D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2656630	NM_001010870.3(TDRD6):c.4878G>A (p.Ser1626=)	TDRD6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656629	NM_001010870.3(TDRD6):c.4295A>G (p.Lys1432Arg)	TDRD6 (K1432R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656628	NM_001010870.3(TDRD6):c.3912A>G (p.Gly1304=)	TDRD6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656627	NM_001010870.3(TDRD6):c.3806C>G (p.Thr1269Arg)	TDRD6 (T1269R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656626	NM_001010870.3(TDRD6):c.2826C>A (p.Thr942=)	TDRD6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656625	NM_001010870.3(TDRD6):c.2403A>C (p.Leu801=)	TDRD6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656624	NM_001010870.3(TDRD6):c.1136A>G (p.Tyr379Cys)	TDRD6 (Y379C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656623	NM_001010870.3(TDRD6):c.693G>A (p.Pro231=)	TDRD6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656622	NM_001010870.3(TDRD6):c.642A>G (p.Thr214=)	TDRD6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656621	NM_001010870.3(TDRD6):c.451C>T (p.Pro151Ser)	TDRD6 (P151S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2621023	NM_001010870.3(TDRD6):c.3287T>C (p.Val1096Ala)	TDRD6 (V1096A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618131	NM_001010870.3(TDRD6):c.1535C>T (p.Thr512Ile)	TDRD6 (T512I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617894	NM_001010870.3(TDRD6):c.6031C>A (p.Pro2011Thr)	TDRD6 (P2011T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617893	NM_001010870.3(TDRD6):c.4640T>C (p.Leu1547Ser)	TDRD6 (L1547S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613348	NM_001010870.3(TDRD6):c.3977A>G (p.Glu1326Gly)	TDRD6 (E1326G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609328	NM_001010870.3(TDRD6):c.1721A>G (p.Asn574Ser)	TDRD6 (N574S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606335	NM_001010870.3(TDRD6):c.60C>G (p.Phe20Leu)	TDRD6 (F20L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604372	NM_001010870.3(TDRD6):c.8C>T (p.Ser3Leu)	TDRD6, TDRD6-AS1 (S3L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2603156	NM_001010870.3(TDRD6):c.127T>A (p.Tyr43Asn)	TDRD6 (Y43N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597643	NM_001010870.3(TDRD6):c.3745C>G (p.Gln1249Glu)	TDRD6 (Q1249E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569925	NM_001010870.3(TDRD6):c.5966C>T (p.Ser1989Leu)	TDRD6 (S1989L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568491	NM_001010870.3(TDRD6):c.5854C>A (p.Gln1952Lys)	TDRD6 (Q1952K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559123	NM_001010870.3(TDRD6):c.494A>T (p.Glu165Val)	TDRD6 (E165V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551488	NM_001010870.3(TDRD6):c.5281A>G (p.Ile1761Val)	TDRD6 (I1761V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546847	NM_001010870.3(TDRD6):c.1252G>A (p.Val418Met)	TDRD6 (V418M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545580	NM_001010870.3(TDRD6):c.5134A>G (p.Ile1712Val)	TDRD6 (I1712V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542031	NM_001010870.3(TDRD6):c.2777C>T (p.Ala926Val)	TDRD6 (A926V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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