ClinVar for Gene (Select 10743) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3378168	NM_030665.4(RAI1):c.2161C>G (p.Pro721Ala)	RAI1 (P721A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3377951	NM_030665.4(RAI1):c.509C>T (p.Ser170Phe)	RAI1 (S170F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3377828	NM_030665.4(RAI1):c.4057C>T (p.Pro1353Ser)	RAI1 (P1353S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3375591	NM_030665.4(RAI1):c.4570A>C (p.Lys1524Gln)	RAI1 (K1524Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3375559	NM_030665.4(RAI1):c.5681A>C (p.Asn1894Thr)	RAI1 (N1894T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3375527	NM_030665.4(RAI1):c.3653C>T (p.Pro1218Leu)	RAI1 (P1218L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3375503	NM_030665.4(RAI1):c.4369G>A (p.Gly1457Arg)	RAI1 (G1457R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3375135	NM_030665.4(RAI1):c.341G>C (p.Gly114Ala)	RAI1 (G114A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3371993	NM_030665.4(RAI1):c.949C>G (p.Gln317Glu)	RAI1 (Q317E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369942	NM_030665.4(RAI1):c.2347G>C (p.Asp783His)	RAI1 (D783H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368389	NM_030665.4(RAI1):c.697G>A (p.Ala233Thr)	RAI1 (A233T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367543	NM_030665.4(RAI1):c.3300G>C (p.Lys1100Asn)	RAI1 (K1100N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361115	NM_030665.4(RAI1):c.4331C>G (p.Pro1444Arg)	RAI1 (P1444R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3360224	NM_030665.4(RAI1):c.1985G>T (p.Gly662Val)	RAI1 (G662V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3360004	NM_030665.4(RAI1):c.613C>G (p.Gln205Glu)	RAI1 (Q205E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3358818	NM_030665.4(RAI1):c.-134A>G	RAI1	Single nucleotide variant (5 prime UTR variant)	RAI1-related disorder	GLikely benign
Select item 3358735	NM_030665.4(RAI1):c.5195C>A (p.Ala1732Asp)	RAI1 (A1732D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3358587	NM_030665.4(RAI1):c.-148-61C>T	RAI1	Single nucleotide variant (intron variant)	RAI1-related disorder	GLikely benign
Select item 3358573	NM_030665.4(RAI1):c.2829G>A (p.Glu943=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3358547	NM_030665.4(RAI1):c.1177A>G (p.Met393Val)	RAI1 (M393V)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3358284	NM_030665.4(RAI1):c.-148-24G>C	RAI1	Single nucleotide variant (intron variant)	RAI1-related disorder	GLikely benign
Select item 3358265	NM_030665.4(RAI1):c.3693G>T (p.Pro1231=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3358193	NM_030665.4(RAI1):c.1392T>C (p.Gly464=)	RAI1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3358017	NM_030665.4(RAI1):c.4563G>A (p.Arg1521=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3357778	NM_030665.4(RAI1):c.1302C>T (p.Ser434=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3357751	NM_030665.4(RAI1):c.-148-56C>T	RAI1	Single nucleotide variant (intron variant)	RAI1-related disorder	GLikely benign
Select item 3357338	NM_030665.4(RAI1):c.-148G>T	RAI1	Single nucleotide variant (5 prime UTR variant)	RAI1-related disorder	GUncertain significance
Select item 3357317	NM_030665.4(RAI1):c.4059T>C (p.Pro1353=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3357285	NM_030665.4(RAI1):c.5436G>T (p.Pro1812=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3357189	NM_030665.4(RAI1):c.3180C>T (p.Leu1060=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3357160	NM_030665.4(RAI1):c.4373T>G (p.Leu1458Arg)	RAI1 (L1458R)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3357149	NM_030665.4(RAI1):c.2688A>G (p.Pro896=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3357042	NM_030665.4(RAI1):c.2805G>A (p.Glu935=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3356720	NM_030665.4(RAI1):c.4260T>C (p.Ser1420=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3356620	NM_030665.4(RAI1):c.2301G>A (p.Lys767=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3356516	NM_030665.4(RAI1):c.2868T>G (p.Pro956=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3356462	NM_030665.4(RAI1):c.3588G>C (p.Glu1196Asp)	RAI1 (E1196D)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3356000	NM_030665.4(RAI1):c.3504C>T (p.Leu1168=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3355970	NM_030665.4(RAI1):c.2009C>T (p.Ser670Phe)	RAI1 (S670F)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355937	NM_030665.4(RAI1):c.555C>T (p.Tyr185=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3355929	NM_030665.4(RAI1):c.-3G>A	RAI1	Single nucleotide variant (5 prime UTR variant)	RAI1-related disorder	GLikely benign
Select item 3355888	NM_030665.4(RAI1):c.119G>T (p.Cys40Phe)	RAI1 (C40F)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355818	NM_030665.4(RAI1):c.1966A>G (p.Ser656Gly)	RAI1 (S656G)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355766	NM_030665.4(RAI1):c.1167C>G (p.His389Gln)	RAI1 (H389Q)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355711	NM_030665.4(RAI1):c.4752G>A (p.Lys1584=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3355656	NM_030665.4(RAI1):c.2834C>G (p.Ser945Cys)	RAI1 (S945C)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355633	NM_030665.4(RAI1):c.4052C>T (p.Ala1351Val)	RAI1 (A1351V)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355372	NM_030665.4(RAI1):c.2253G>T (p.Leu751=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3355336	NM_030665.4(RAI1):c.4775C>T (p.Thr1592Ile)	RAI1 (T1592I)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355215	NM_030665.4(RAI1):c.707A>T (p.Tyr236Phe)	RAI1 (Y236F)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355191	NM_030665.4(RAI1):c.4078T>C (p.Ser1360Pro)	RAI1 (S1360P)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3355190	NM_030665.4(RAI1):c.1782T>C (p.Cys594=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3355106	NM_030665.4(RAI1):c.2619C>T (p.Ser873=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3354945	NM_030665.4(RAI1):c.335A>G (p.Tyr112Cys)	RAI1 (Y112C)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3354882	NM_030665.4(RAI1):c.366G>C (p.Gly122=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3354761	NM_030665.4(RAI1):c.3540C>T (p.Asn1180=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3354601	NM_030665.4(RAI1):c.2418G>C (p.Leu806Phe)	RAI1 (L806F)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3354485	NM_030665.4(RAI1):c.-148-7T>C	RAI1	Single nucleotide variant (intron variant)	RAI1-related disorder	GLikely benign
Select item 3354473	NM_030665.4(RAI1):c.4839T>C (p.Val1613=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3354077	NM_030665.4(RAI1):c.3341C>T (p.Ala1114Val)	RAI1 (A1114V)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3354051	NM_030665.4(RAI1):c.4097G>A (p.Arg1366His)	RAI1 (R1366H)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3353872	NM_030665.4(RAI1):c.4221C>T (p.Ser1407=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3353405	NM_030665.4(RAI1):c.4179T>C (p.Thr1393=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3353069	NM_030665.4(RAI1):c.5178A>G (p.Glu1726=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3353036	NM_030665.4(RAI1):c.5097T>C (p.Leu1699=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3353025	NM_030665.4(RAI1):c.3137G>C (p.Arg1046Pro)	RAI1 (R1046P)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3352921	NM_030665.4(RAI1):c.5214A>G (p.Arg1738=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3352790	NM_030665.4(RAI1):c.-148-22G>A	RAI1	Single nucleotide variant (intron variant)	RAI1-related disorder	GLikely benign
Select item 3351749	NM_030665.4(RAI1):c.-132C>T	RAI1	Single nucleotide variant (5 prime UTR variant)	RAI1-related disorder	GLikely benign
Select item 3351637	NM_030665.4(RAI1):c.5124T>C (p.Pro1708=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3351522	NM_030665.4(RAI1):c.1071T>C (p.Ser357=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3351518	NM_030665.4(RAI1):c.5109T>C (p.Cys1703=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3351474	NM_030665.4(RAI1):c.4830A>G (p.Ile1610Met)	RAI1 (I1610M)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3351419	NM_030665.4(RAI1):c.5208T>G (p.Leu1736=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3351198	NM_030665.4(RAI1):c.-5G>C	RAI1	Single nucleotide variant (5 prime UTR variant)	RAI1-related disorder	GLikely benign
Select item 3351140	NM_030665.4(RAI1):c.1998C>G (p.Ala666=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3351063	NM_030665.4(RAI1):c.1521C>T (p.Ser507=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3351024	NM_030665.4(RAI1):c.4512G>A (p.Leu1504=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3350581	NM_030665.4(RAI1):c.1377G>A (p.Val459=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3350470	NM_030665.4(RAI1):c.4488C>G (p.Gly1496=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3350401	NM_030665.4(RAI1):c.2158G>C (p.Asp720His)	RAI1 (D720H)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3350237	NM_030665.4(RAI1):c.654C>A (p.Thr218=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3350109	NM_030665.4(RAI1):c.3826C>G (p.Pro1276Ala)	RAI1 (P1276A)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349883	NM_030665.4(RAI1):c.5417_5418del (p.Glu1806fs)	RAI1 (E1806fs)	Deletion (frameshift variant)	RAI1-related disorder	GLikely pathogenic
Select item 3349816	NM_030665.4(RAI1):c.4375T>A (p.Ser1459Thr)	RAI1 (S1459T)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349780	NM_030665.4(RAI1):c.3284G>T (p.Gly1095Val)	RAI1 (G1095V)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349696	NM_030665.4(RAI1):c.5171G>A (p.Arg1724Gln)	RAI1 (R1724Q)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349658	NM_030665.4(RAI1):c.1176C>G (p.Phe392Leu)	RAI1 (F392L)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349624	NM_030665.4(RAI1):c.449C>T (p.Ala150Val)	RAI1 (A150V)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349618	NM_030665.4(RAI1):c.652_654del (p.Thr218del)	RAI1 (T218del)	Deletion (inframe_deletion)	RAI1-related disorder	GUncertain significance
Select item 3349606	NM_030665.4(RAI1):c.2274G>A (p.Trp758Ter)	RAI1 (W758*)	Single nucleotide variant (nonsense)	RAI1-related disorder	GPathogenic
Select item 3349581	NM_030665.4(RAI1):c.2322G>C (p.Lys774Asn)	RAI1 (K774N)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349550	NM_030665.4(RAI1):c.3273C>G (p.Ala1091=)	RAI1	Single nucleotide variant (synonymous variant)	RAI1-related disorder	GLikely benign
Select item 3349273	NM_030665.4(RAI1):c.2149C>T (p.Pro717Ser)	RAI1 (P717S)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349259	NM_030665.4(RAI1):c.2095C>A (p.Pro699Thr)	RAI1 (P699T)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349122	NM_030665.4(RAI1):c.5080G>A (p.Ala1694Thr)	RAI1 (A1694T)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3349064	NM_030665.4(RAI1):c.5258dup (p.Pro1754fs)	RAI1 (P1754fs)	Duplication (frameshift variant)	RAI1-related disorder	GLikely pathogenic
Select item 3348979	NM_030665.4(RAI1):c.3816G>T (p.Arg1272Ser)	RAI1 (R1272S)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3348934	NM_030665.4(RAI1):c.4130G>T (p.Gly1377Val)	RAI1 (G1377V)	Single nucleotide variant (missense variant)	RAI1-related disorder	GUncertain significance
Select item 3348799	NM_030665.4(RAI1):c.3937_3938delinsT (p.Ala1313fs)	RAI1 (A1313fs)	Indel (frameshift variant)	RAI1-related disorder	GLikely pathogenic

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