ClinVar for Gene (Select 4938) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3301793	NM_016816.4(OAS1):c.113G>A (p.Cys38Tyr)	LOC130008812, OAS1 (C38Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3301792	NM_016816.4(OAS1):c.919A>G (p.Asn307Asp)	OAS1 (N149D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3301791	NM_016816.4(OAS1):c.70A>C (p.Thr24Pro)	LOC130008812, OAS1 (T24P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3244426	NC_000012.11:g.(?_113344845)_(113357358_?)dup	OAS1	Duplication	not provided	GUncertain significance
Select item 3203635	NM_016816.4(OAS1):c.1164C>T (p.Thr388=)	OAS1 (P348S +2 more)	Single nucleotide variant (missense variant +4 more)	not specified	GLikely benign
Select item 3068076	NM_016816.4(OAS1):c.609del (p.Lys204fs)	OAS1 (K204fs +1 more)	Deletion (frameshift variant +2 more)	Pulmonary alveolar proteinosis with hypogammaglobulinemia	GUncertain significance
Select item 3058877	NM_001320151.2(OAS1):c.1072del (p.Thr358fs)	OAS1 (T350fs +1 more)	Deletion (frameshift variant +1 more)	OAS1-related disorder	GBenign
Select item 3056096	NM_016816.4(OAS1):c.174G>A (p.Val58=)	LOC130008812, OAS1	Single nucleotide variant (synonymous variant +1 more)	OAS1-related disorder	GLikely benign
Select item 3046846	NM_016816.4(OAS1):c.1038+64T>C	OAS1	Single nucleotide variant (3 prime UTR variant +2 more)	OAS1-related disorder	GLikely benign
Select item 3039452	NM_016816.4(OAS1):c.*51C>T	OAS1 (L228F +2 more)	Single nucleotide variant (missense variant +3 more)	OAS1-related disorder	GLikely benign
Select item 3017208	NM_016816.4(OAS1):c.234G>A (p.Leu78=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3006175	NM_016816.4(OAS1):c.774C>A (p.Val258=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3003885	NM_016816.4(OAS1):c.469+23dup	OAS1	Duplication (intron variant)	not provided	GBenign
Select item 3002659	NM_016816.4(OAS1):c.727G>A (p.Gly243Arg)	OAS1 (G85R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3000486	NM_016816.4(OAS1):c.546A>G (p.Lys182=)	OAS1 (R167G)	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3000113	NM_016816.4(OAS1):c.60C>G (p.Leu20=)	LOC130008812, OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2996649	NM_016816.4(OAS1):c.39del (p.Asp13fs)	LOC130008812, OAS1 (D13fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2994767	NM_016816.4(OAS1):c.1039-12T>A	OAS1	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 2993352	NM_016816.4(OAS1):c.724C>T (p.Arg242Ter)	OAS1 (R234* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2990873	NM_016816.4(OAS1):c.884+16A>G	OAS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2987059	NM_016816.4(OAS1):c.386C>A (p.Pro129His)	OAS1 (P129H)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2984501	NM_016816.4(OAS1):c.463G>A (p.Ala155Thr)	OAS1 (A155T)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2984500	NM_016816.4(OAS1):c.456C>G (p.Ala152=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2982167	NM_016816.4(OAS1):c.785T>A (p.Val262Asp)	OAS1 (V104D +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2978314	NM_016816.4(OAS1):c.455C>A (p.Ala152Asp)	OAS1 (A152D)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2970365	NM_016816.4(OAS1):c.80G>A (p.Arg27His)	LOC130008812, OAS1 (R27H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2960627	NM_016816.4(OAS1):c.828T>C (p.Tyr276=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2960217	NM_016816.4(OAS1):c.333A>G (p.Arg111=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2956662	NM_016816.4(OAS1):c.393G>A (p.Ala131=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2954960	NM_016816.4(OAS1):c.207C>A (p.Thr69=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2909878	NM_016816.4(OAS1):c.374G>A (p.Arg125His)	OAS1 (R125H)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2906561	NM_016816.4(OAS1):c.63G>A (p.Leu21=)	LOC130008812, OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2905716	NM_016816.4(OAS1):c.311G>A (p.Arg104Lys)	OAS1 (R104K)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2902844	NM_016816.4(OAS1):c.402C>T (p.Phe134=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2902193	NM_016816.4(OAS1):c.356T>A (p.Phe119Tyr)	OAS1 (F119Y)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2876409	NM_016816.4(OAS1):c.654+8C>G	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GUncertain significance
Select item 2876408	NM_016816.4(OAS1):c.470-14T>C	OAS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872992	NM_016816.4(OAS1):c.844A>G (p.Ile282Val)	OAS1 (I282V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2870559	NM_016816.4(OAS1):c.470-19G>A	OAS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869968	NM_016816.4(OAS1):c.347C>T (p.Ser116Phe)	OAS1 (S116F)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2866408	NM_016816.4(OAS1):c.894C>A (p.Ile298=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2866242	NM_016816.4(OAS1):c.280C>T (p.Arg94Cys)	OAS1 (R94C)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2863747	NM_016816.4(OAS1):c.1080G>C (p.Arg360Ser)	OAS1 (R202S +2 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2858370	NM_016816.4(OAS1):c.747C>G (p.Phe249Leu)	OAS1 (F249L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2854283	NM_016816.4(OAS1):c.1059C>A (p.Asp353Glu)	OAS1 (D195E +2 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2825794	NM_016816.4(OAS1):c.287G>C (p.Gly96Ala)	OAS1 (G96A)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2821180	NM_016816.4(OAS1):c.374G>T (p.Arg125Leu)	OAS1 (R125L)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2821005	NM_016816.4(OAS1):c.1179G>C (p.Glu393Asp)	OAS1 (E393D +5 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2818042	NM_016816.4(OAS1):c.792C>T (p.Asn264=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2817440	NM_016816.4(OAS1):c.32C>A (p.Ser11Tyr)	LOC130008812, OAS1 (S11Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2808369	NM_016816.4(OAS1):c.1037T>C (p.Leu346Pro)	OAS1 (L188P +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2806394	NM_016816.4(OAS1):c.186C>T (p.Gly62=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2805264	NM_016816.4(OAS1):c.884+12C>T	OAS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2805076	NM_016816.4(OAS1):c.356T>C (p.Phe119Ser)	OAS1 (F119S)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2792554	NM_016816.4(OAS1):c.153C>T (p.Tyr51=)	LOC130008812, OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2790440	NM_016816.4(OAS1):c.483C>T (p.Gly161=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2788193	NM_016816.4(OAS1):c.938C>G (p.Pro313Arg)	OAS1 (P305R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2783843	NM_016816.4(OAS1):c.787A>G (p.Ile263Val)	OAS1 (I255V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2781224	NM_016816.4(OAS1):c.500C>G (p.Pro167Arg)	OAS1 (P167R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2755539	NM_016816.4(OAS1):c.1032T>C (p.Ile344=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2741342	NM_016816.4(OAS1):c.675G>A (p.Lys225=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2734192	NM_016816.4(OAS1):c.1022G>A (p.Ser341Asn)	OAS1 (S183N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2729941	NM_016816.4(OAS1):c.424G>A (p.Gly142Arg)	OAS1 (G142R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2706061	NM_016816.4(OAS1):c.1062T>A (p.Asp354Glu)	OAS1 (D346E +2 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 2700405	NM_016816.4(OAS1):c.12C>G (p.Leu4=)	LOC130008812, OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2699530	NM_016816.4(OAS1):c.86A>G (p.Gln29Arg)	LOC130008812, OAS1 (Q29R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2692582	NM_016816.4(OAS1):c.287G>A (p.Gly96Glu)	OAS1 (G96E)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2688063	NM_001320151.2(OAS1):c.1039-39C>T	OAS1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687938	NM_001320151.2(OAS1):c.*32G>C	OAS1	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GBenign
Select item 2643345	NM_016816.4(OAS1):c.654+17A>T	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2636588	NM_001320151.2(OAS1):c.1040T>C (p.Val347Ala)	OAS1 (V339A +1 more)	Single nucleotide variant (missense variant +1 more)	OAS1-related disorder	GUncertain significance
Select item 2634020	NM_016816.4(OAS1):c.470-3C>G	OAS1	Single nucleotide variant (intron variant)	OAS1-related disorder	GUncertain significance
Select item 2633265	NM_016816.4(OAS1):c.1193C>T (p.Thr398Ile)	OAS1 (T240I +2 more)	Single nucleotide variant (synonymous variant +4 more)	OAS1-related disorder	GUncertain significance
Select item 2576592	NM_016816.4(OAS1):c.654+3A>G	OAS1 (M204V)	Single nucleotide variant (missense variant +2 more)	Pulmonary alveolar proteinosis with hypogammaglobulinemia	GUncertain significance
Select item 2547765	NM_016816.4(OAS1):c.629G>T (p.Arg210Leu)	OAS1 (R210L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2545140	NM_016816.4(OAS1):c.401T>C (p.Phe134Ser)	OAS1 (F134S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2532564	NM_016816.4(OAS1):c.143G>A (p.Gly48Asp)	LOC130008812, OAS1 (G48D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2523620	NM_016816.4(OAS1):c.928G>A (p.Gly310Ser)	OAS1 (G310S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457959	NM_016816.4(OAS1):c.625A>G (p.Ile209Val)	OAS1 (H193R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 2416782	NM_016816.4(OAS1):c.884+6C>T	OAS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2415386	NM_016816.4(OAS1):c.639G>A (p.Lys213=)	OAS1 (A198T)	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 2409082	NM_016816.4(OAS1):c.907G>C (p.Asp303His)	OAS1 (D295H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267072	NM_016816.4(OAS1):c.213A>T (p.Arg71Ser)	OAS1 (R71S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2194393	NM_016816.4(OAS1):c.535G>A (p.Asp179Asn)	OAS1 (D179N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2194276	NM_016816.4(OAS1):c.905C>T (p.Ala302Val)	OAS1 (A302V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2192658	NM_016816.4(OAS1):c.915A>G (p.Thr305=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2192361	NM_016816.4(OAS1):c.623T>G (p.Leu208Arg)	OAS1 (L208R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2191320	NM_016816.4(OAS1):c.962A>G (p.Gln321Arg)	OAS1 (Q163R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2191005	NM_016816.4(OAS1):c.429G>C (p.Glu143Asp)	OAS1 (E143D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2186728	NM_016816.4(OAS1):c.469+9T>C	OAS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2186571	NM_016816.4(OAS1):c.867G>A (p.Arg289=)	OAS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2184057	NM_016816.4(OAS1):c.79C>T (p.Arg27Cys)	LOC130008812, OAS1 (R27C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2180687	NM_016816.4(OAS1):c.424G>C (p.Gly142Arg)	OAS1 (G142R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2180440	NM_016816.4(OAS1):c.977G>A (p.Trp326Ter)	OAS1 (W168* +2 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2178163	NM_016816.4(OAS1):c.437A>T (p.Glu146Val)	OAS1 (E146V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2169099	NM_016816.4(OAS1):c.53A>G (p.Asp18Gly)	LOC130008812, OAS1 (D18G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2162365	NM_016816.4(OAS1):c.348C>A (p.Ser116=)	OAS1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2151207	NM_016816.4(OAS1):c.926G>A (p.Gly309Asp)	OAS1 (G301D +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2144408	NM_016816.4(OAS1):c.746T>C (p.Phe249Ser)	OAS1 (F91S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2141137	NM_016816.4(OAS1):c.655-10C>T	OAS1	Single nucleotide variant (intron variant)	not provided	GLikely benign

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