TET2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	ABHD18, ADAD1 +661 more	Copy number gain	See cases	GPathogenic
Select item 3030596	NC_000004.12:g.104314617A>T	TET2	Single nucleotide variant	TET2-related condition	GLikely benign
Select item 800353	NC_000004.12:g.104314621_104314622insG	TET2	Insertion	Multiple myeloma	GLikely pathogenic
Select item 1234506	NM_001127208.3(TET2):c.-46-63ATAG[4]	TET2, TET2-AS1	Microsatellite (intron variant)	not specified +1 more	GBenign
Select item 2970734	NM_001127208.3(TET2):c.9G>A (p.Gln3=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2082675	NM_001127208.3(TET2):c.15A>G (p.Arg5=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2918006	NM_001127208.3(TET2):c.21C>T (p.Asn7=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2061159	NM_001127208.3(TET2):c.22C>G (p.His8Asp)	TET2, TET2-AS1 (H8D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 753440	NM_001127208.3(TET2):c.36C>T (p.Asn12=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2044059	NM_001127208.3(TET2):c.37A>C (p.Arg13=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2870393	NM_001127208.3(TET2):c.60A>C (p.Pro20=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2899265	NM_001127208.3(TET2):c.74G>T (p.Cys25Phe)	TET2, TET2-AS1 (C25F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1995846	NM_001127208.3(TET2):c.80C>G (p.Thr27Arg)	TET2, TET2-AS1 (T27R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 135316	NM_001127208.3(TET2):c.86C>G (p.Pro29Arg)	TET2, TET2-AS1 (P29R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1700440	NM_001127208.3(TET2):c.95C>T (p.Thr32Ile)	TET2, TET2-AS1 (T32I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 135308	NM_001127208.3(TET2):c.100C>T (p.Leu34Phe)	TET2, TET2-AS1 (L34F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1996923	NM_001127208.3(TET2):c.113G>T (p.Ser38Ile)	TET2, TET2-AS1 (S38I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2002693	NM_001127208.3(TET2):c.116C>T (p.Pro39Leu)	TET2, TET2-AS1 (P39L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2708217	NM_001127208.3(TET2):c.171C>T (p.Phe57=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3021870	NM_001127208.3(TET2):c.180T>C (p.Tyr60=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010277	NM_001127208.3(TET2):c.196A>T (p.Met66Leu)	TET2, TET2-AS1 (M66L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 135322	NM_001127208.3(TET2):c.197T>C (p.Met66Thr)	TET2, TET2-AS1 (M66T)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2986146	NM_001127208.3(TET2):c.240A>G (p.Gln80=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2978958	NM_001127208.3(TET2):c.251G>T (p.Gly84Val)	TET2, TET2-AS1 (G84V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2813563	NM_001127208.3(TET2):c.262T>C (p.Cys88Arg)	TET2, TET2-AS1 (C88R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3049831	NM_001127208.3(TET2):c.273T>C (p.Asn91=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition	GLikely benign
Select item 1940758	NM_001127208.3(TET2):c.286C>T (p.Arg96Cys)	TET2, TET2-AS1 (R96C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2831038	NM_001127208.3(TET2):c.290_291dup (p.Val98fs)	TET2, TET2-AS1 (V98fs)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 2012161	NM_001127208.3(TET2):c.294_295insCA (p.Ser99fs)	TET2, TET2-AS1 (S99fs)	Insertion (frameshift variant)	not provided	GUncertain significance
Select item 2857035	NM_001127208.3(TET2):c.299A>G (p.Glu100Gly)	TET2, TET2-AS1 (E100G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2978063	NM_001127208.3(TET2):c.302C>T (p.Pro101Leu)	TET2, TET2-AS1 (P101L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2756229	NM_001127208.3(TET2):c.323A>T (p.Gln108Leu)	TET2, TET2-AS1 (Q108L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2026892	NM_001127208.3(TET2):c.336G>T (p.Leu112Phe)	TET2, TET2-AS1 (L112F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2857133	NM_001127208.3(TET2):c.346del (p.Gln116fs)	TET2, TET2-AS1 (Q116fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2873113	NM_001127208.3(TET2):c.346C>T (p.Gln116Ter)	TET2, TET2-AS1 (Q116*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1978379	NM_001127208.3(TET2):c.356A>G (p.Asn119Ser)	TET2, TET2-AS1 (N119S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2635058	NM_001127208.3(TET2):c.368G>A (p.Arg123His)	TET2, TET2-AS1 (R123H)	Single nucleotide variant (missense variant)	TET2-related condition	GUncertain significance
Select item 2083650	NM_001127208.3(TET2):c.376G>A (p.Gly126Arg)	TET2, TET2-AS1 (G126R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2476927	NM_001127208.3(TET2):c.410G>C (p.Ser137Thr)	TET2, TET2-AS1 (S137T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1899046	NM_001127208.3(TET2):c.413A>T (p.Gln138Leu)	TET2, TET2-AS1 (Q138L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1910894	NM_001127208.3(TET2):c.418A>G (p.Asn140Asp)	TET2, TET2-AS1 (N140D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2654997	NM_001127208.3(TET2):c.426C>T (p.Ser142=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 135320	NM_001127208.3(TET2):c.434G>A (p.Ser145Asn)	TET2, TET2-AS1 (S145N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2474774	NM_001127208.3(TET2):c.435T>G (p.Ser145Arg)	TET2, TET2-AS1 (S145R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2747069	NM_001127208.3(TET2):c.441G>C (p.Lys147Asn)	TET2, TET2-AS1 (K147N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2834214	NM_001127208.3(TET2):c.452_453del (p.Val151fs)	TET2, TET2-AS1 (V151fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 3006280	NM_001127208.3(TET2):c.468A>G (p.Gln156=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1915496	NM_001127208.3(TET2):c.478G>A (p.Val160Ile)	TET2, TET2-AS1 (V160I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2790450	NM_001127208.3(TET2):c.483dup (p.Asp162fs)	TET2, TET2-AS1 (D162fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 135315	NM_001127208.3(TET2):c.521C>A (p.Pro174His)	TET2, TET2-AS1 (P174H)	Single nucleotide variant (missense variant)	TET2-related condition +2 more	GConflicting classifications of pathogenicity
Select item 2404452	NM_001127208.3(TET2):c.528T>A (p.Asn176Lys)	TET2, TET2-AS1 (N176K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2819430	NM_001127208.3(TET2):c.553C>T (p.Gln185Ter)	TET2, TET2-AS1 (Q185*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2904214	NM_001127208.3(TET2):c.574T>C (p.Tyr192His)	TET2, TET2-AS1 (Y192H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 746874	NM_001127208.3(TET2):c.606C>T (p.Asn202=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2966846	NM_001127208.3(TET2):c.615G>A (p.Val205=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2895045	NM_001127208.3(TET2):c.651C>T (p.Ser217=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 135321	NM_001127208.3(TET2):c.652G>A (p.Val218Met)	TET2, TET2-AS1 (V218M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2100877	NM_001127208.3(TET2):c.668_670del (p.Gly223del)	TET2, TET2-AS1 (G223del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2654998	NM_001127208.3(TET2):c.674T>C (p.Leu225Pro)	TET2, TET2-AS1 (L225P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1879612	NM_001127208.3(TET2):c.685dup (p.Thr229fs)	TET2, TET2-AS1 (T229fs)	Duplication (frameshift variant)	Immunodeficiency 75 +1 more	GConflicting classifications of pathogenicity
Select item 2277331	NM_001127208.3(TET2):c.710G>A (p.Cys237Tyr)	TET2, TET2-AS1 (C237Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2794803	NM_001127208.3(TET2):c.720T>C (p.Ile240=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1926833	NM_001127208.3(TET2):c.723G>A (p.Ala241=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1338088	NM_001127208.3(TET2):c.723G>T (p.Ala241=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 1329593	NM_001127208.3(TET2):c.744C>A (p.His248Gln)	TET2, TET2-AS1 (H248Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2793149	NM_001127208.3(TET2):c.745A>G (p.Ile249Val)	TET2, TET2-AS1 (I249V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2108400	NM_001127208.3(TET2):c.782C>T (p.Ser261Phe)	TET2, TET2-AS1 (S261F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2893852	NM_001127208.3(TET2):c.792C>T (p.Ile264=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970536	NM_001127208.3(TET2):c.799C>T (p.Pro267Ser)	TET2, TET2-AS1 (P267S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2149887	NM_001127208.3(TET2):c.804G>C (p.Ser268=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition +1 more	GLikely benign
Select item 2631697	NM_001127208.3(TET2):c.806A>T (p.His269Leu)	TET2, TET2-AS1 (H269L)	Single nucleotide variant (missense variant)	TET2-related condition	GUncertain significance
Select item 1936676	NM_001127208.3(TET2):c.822del (p.Asn275fs)	TET2, TET2-AS1 (N275fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2143552	NM_001127208.3(TET2):c.825T>G (p.Asn275Lys)	TET2, TET2-AS1 (N275K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3022595	NM_001127208.3(TET2):c.829G>A (p.Ala277Thr)	TET2, TET2-AS1 (A277T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2712187	NM_001127208.3(TET2):c.831A>C (p.Ala277=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000171	NM_001127208.3(TET2):c.832C>T (p.Gln278Ter)	TET2, TET2-AS1 (Q278*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2859380	NM_001127208.3(TET2):c.834del (p.Thr279fs)	TET2, TET2-AS1 (T279fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2798192	NM_001127208.3(TET2):c.860del (p.Lys287fs)	TET2, TET2-AS1 (K287fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 3011872	NM_001127208.3(TET2):c.864A>G (p.Pro288=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 737539	NM_001127208.3(TET2):c.879T>C (p.Ser293=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2010325	NM_001127208.3(TET2):c.889GATGCTGAT[1] (p.297DAD[1])	TET2, TET2-AS1	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 135307	NM_001127208.3(TET2):c.899A>G (p.Asp300Gly)	TET2, TET2-AS1 (D300G)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2363063	NM_001127208.3(TET2):c.917A>G (p.Lys306Arg)	TET2, TET2-AS1 (K306R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 135325	NM_001127208.3(TET2):c.920T>G (p.Leu307Arg)	TET2, TET2-AS1 (L307R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2889009	NM_001127208.3(TET2):c.936T>C (p.Asn312=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2804562	NM_001127208.3(TET2):c.949C>T (p.Gln317Ter)	TET2, TET2-AS1 (Q317*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2993463	NM_001127208.3(TET2):c.951G>C (p.Gln317His)	TET2, TET2-AS1 (Q317H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 135301	NM_001127208.3(TET2):c.959AAC[1] (p.Gln321del)	TET2, TET2-AS1 (Q321del)	Microsatellite (inframe_deletion)	not specified	Gnot provided
Select item 2023957	NM_001127208.3(TET2):c.961del (p.Gln321fs)	TET2, TET2-AS1 (Q321fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2006580	NM_001127208.3(TET2):c.967CAA[2] (p.Gln325del)	TET2, TET2-AS1 (Q325del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2052183	NM_001127208.3(TET2):c.972A>G (p.Gln324=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2146953	NM_001127208.3(TET2):c.978A>G (p.Lys326=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2045553	NM_001127208.3(TET2):c.1041G>A (p.Ala347=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2920213	NM_001127208.3(TET2):c.1044T>C (p.Ser348=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2133052	NM_001127208.3(TET2):c.1061C>G (p.Ser354Ter)	TET2, TET2-AS1 (S354*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 135317	NM_001127208.3(TET2):c.1064G>A (p.Gly355Asp)	TET2-AS1, TET2 (G355D)	Single nucleotide variant (missense variant)	TET2-related condition +1 more	GBenign
Select item 2889239	NM_001127208.3(TET2):c.1074C>T (p.Ser358=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 135309	NM_001127208.3(TET2):c.1088C>T (p.Pro363Leu)	TET2, TET2-AS1 (P363L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2173854	NM_001127208.3(TET2):c.1105C>T (p.Arg369Trp)	TET2, TET2-AS1 (R369W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2859816	NM_001127208.3(TET2):c.1132_1133del (p.Gly378fs)	TET2, TET2-AS1 (G378fs)	Deletion (frameshift variant)	not provided	GPathogenic

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