Related gene-specific medical variations for Gene (Select 54790) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052524	NM_001127208.3(TET2):c.5883G>A (p.Glu1961=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition	GLikely benign
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 3048802	NM_001127208.3(TET2):c.4053T>C (p.Tyr1351=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition	GLikely benign
Select item 3047695	NM_001127208.3(TET2):c.1594T>C (p.Leu532=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition	GLikely benign
Select item 3047688	NM_001127208.3(TET2):c.3711G>A (p.Pro1237=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition	GLikely benign
Select item 3030596	NC_000004.12:g.104314617A>T	TET2	Single nucleotide variant	TET2-related condition	GLikely benign
Select item 3025947	NM_001127208.3(TET2):c.2282C>T (p.Pro761Leu)	TET2, TET2-AS1 (P761L)	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 3022021	NM_001127208.3(TET2):c.5650A>G (p.Thr1884Ala)	TET2, TET2-AS1 (T1884A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 3019863	NM_001127208.3(TET2):c.2572A>G (p.Lys858Glu)	TET2, TET2-AS1 (K858E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3018322	NM_001127208.3(TET2):c.1808A>G (p.Lys603Arg)	TET2, TET2-AS1 (K603R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3017694	NM_001127208.3(TET2):c.3088C>T (p.Gln1030Ter)	TET2, TET2-AS1 (Q1030*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3017246	NM_001127208.3(TET2):c.1264G>T (p.Gly422Ter)	TET2, TET2-AS1 (G422*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3016272	NM_001127208.3(TET2):c.5131A>G (p.Ile1711Val)	TET2, TET2-AS1 (I1711V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3016179	NM_001127208.3(TET2):c.3728A>G (p.Lys1243Arg)	TET2, TET2-AS1 (K1243R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3013217	NM_001127208.3(TET2):c.1333C>T (p.Leu445Phe)	TET2, TET2-AS1 (L445F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3013093	NM_001127208.3(TET2):c.3812dup (p.Cys1271fs)	TET2, TET2-AS1 (C1271fs)	Duplication (frameshift variant)	not provided	GPathogenic
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 3011065	NM_001127208.3(TET2):c.3920G>A (p.Arg1307Lys)	TET2, TET2-AS1 (R1307K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3010365	NM_001127208.3(TET2):c.2370G>A (p.Gln790=)	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 3009391	NM_001127208.3(TET2):c.5611A>G (p.Ile1871Val)	TET2, TET2-AS1 (I1871V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3008722	NM_001127208.3(TET2):c.3946C>A (p.Pro1316Thr)	TET2, TET2-AS1 (P1316T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3007151	NM_001127208.3(TET2):c.1572G>A (p.Glu524=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006343	NM_001127208.3(TET2):c.4188C>T (p.Cys1396=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 3005732	NM_001127208.3(TET2):c.2928G>A (p.Gln976=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005645	NM_001127208.3(TET2):c.3172A>G (p.Met1058Val)	TET2, TET2-AS1 (M1058V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3005068	NM_001127208.3(TET2):c.3954+19G>A	TET2-AS1, TET2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3003215	NM_001127208.3(TET2):c.3230A>G (p.His1077Arg)	TET2-AS1, TET2 (H1077R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003006	NM_001127208.3(TET2):c.5589C>T (p.Ala1863=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000441	NM_001127208.3(TET2):c.5835T>A (p.His1945Gln)	TET2, TET2-AS1 (H1945Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 3000046	NM_001127208.3(TET2):c.4936C>T (p.Leu1646=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2998209	NM_001127208.3(TET2):c.3142C>G (p.Leu1048Val)	TET2, TET2-AS1 (L1048V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2997966	NM_001127208.3(TET2):c.5106G>A (p.Gln1702=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2997649	NM_001127208.3(TET2):c.4075C>T (p.Arg1359Cys)	TET2, TET2-AS1 (R1359C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2997339	NM_001127208.3(TET2):c.1912A>G (p.Met638Val)	TET2, TET2-AS1 (M638V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2995574	NM_001127208.3(TET2):c.2861G>T (p.Trp954Leu)	TET2-AS1, TET2 (W954L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2995016	NM_001127208.3(TET2):c.2185C>T (p.Gln729Ter)	TET2, TET2-AS1 (Q729*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2994515	NM_001127208.3(TET2):c.1733A>G (p.His578Arg)	TET2, TET2-AS1 (H578R)	Single nucleotide variant (missense variant)	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 2992846	NM_001127208.3(TET2):c.3770C>T (p.Thr1257Met)	TET2, TET2-AS1 (T1257M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2992356	NM_001127208.3(TET2):c.1834C>T (p.Pro612Ser)	TET2, TET2-AS1 (P612S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991343	NM_001127208.3(TET2):c.4160A>G (p.Asn1387Ser)	TET2, TET2-AS1 (N1387S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2989680	NM_001127208.3(TET2):c.4314A>G (p.Lys1438=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2988875	NM_001127208.3(TET2):c.5956A>G (p.Thr1986Ala)	TET2, TET2-AS1 (T1986A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2987588	NM_001127208.3(TET2):c.3955-3_3955-2insGTAT	TET2, TET2-AS1	Insertion (splice acceptor variant)	not provided	GUncertain significance
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 2984265	NM_001127208.3(TET2):c.5791G>A (p.Glu1931Lys)	TET2, TET2-AS1 (E1931K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2982675	NM_001127208.3(TET2):c.4008A>G (p.Thr1336=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2981463	NM_001127208.3(TET2):c.3659C>T (p.Thr1220Ile)	TET2, TET2-AS1 (T1220I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2980416	NM_001127208.3(TET2):c.3803+19C>G	TET2, TET2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980085	NM_001127208.3(TET2):c.3798T>C (p.Asn1266=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979620	NM_001127208.3(TET2):c.4354C>A (p.Arg1452=)	TET2-AS1, TET2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979375	NM_001127208.3(TET2):c.3317_3318del (p.Glu1106fs)	TET2, TET2-AS1 (E1106fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
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 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 2976439	NM_001127208.3(TET2):c.4435C>G (p.Leu1479Val)	TET2, TET2-AS1 (L1479V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975319	NM_001127208.3(TET2):c.5142T>C (p.Asn1714=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2973626	NM_001127208.3(TET2):c.1453G>T (p.Val485Leu)	TET2, TET2-AS1 (V485L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2972914	NM_001127208.3(TET2):c.3043A>G (p.Ser1015Gly)	TET2, TET2-AS1 (S1015G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2972405	NM_001127208.3(TET2):c.4790T>C (p.Phe1597Ser)	TET2, TET2-AS1 (F1597S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 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 2969609	NM_001127208.3(TET2):c.3955-11A>G	TET2, TET2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969381	NM_001127208.3(TET2):c.4275C>T (p.Asp1425=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2967075	NM_001127208.3(TET2):c.1277T>C (p.Leu426Pro)	TET2, TET2-AS1 (L426P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 2966335	NM_001127208.3(TET2):c.3595-13G>A	TET2, TET2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965800	NM_001127208.3(TET2):c.3954+16dup	TET2, TET2-AS1	Duplication (intron variant)	not provided	GLikely benign
Select item 2965264	NM_001127208.3(TET2):c.5259T>C (p.Asn1753=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2961256	NM_001127208.3(TET2):c.4538-13A>T	TET2, TET2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959566	NM_001127208.3(TET2):c.3399C>T (p.Cys1133=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2959390	NM_001127208.3(TET2):c.3202C>A (p.Gln1068Lys)	TET2, TET2-AS1 (Q1068K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2958196	NM_001127208.3(TET2):c.5529C>A (p.Asn1843Lys)	TET2, TET2-AS1 (N1843K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957407	NM_001127208.3(TET2):c.2181A>G (p.Ala727=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955916	NM_001127208.3(TET2):c.4776C>T (p.Thr1592=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955434	NM_001127208.3(TET2):c.4319G>A (p.Arg1440Gln)	TET2, TET2-AS1 (R1440Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 2918006	NM_001127208.3(TET2):c.21C>T (p.Asn7=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2915643	NM_001127208.3(TET2):c.4964C>T (p.Pro1655Leu)	TET2, TET2-AS1 (P1655L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2910611	NM_001127208.3(TET2):c.4625_4645del (p.Gln1542_Gln1548del)	TET2, TET2-AS1	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2908797	NM_001127208.3(TET2):c.3738G>A (p.Ser1246=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2908438	NM_001127208.3(TET2):c.5697C>T (p.Leu1899=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	TET2-related condition +1 more	GLikely benign
Select item 2907735	NM_001127208.3(TET2):c.1422G>A (p.Pro474=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906762	NM_001127208.3(TET2):c.4715G>C (p.Arg1572Pro)	TET2, TET2-AS1 (R1572P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2905361	NM_001127208.3(TET2):c.5745T>C (p.Ala1915=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2904964	NM_001127208.3(TET2):c.2683G>A (p.Val895Ile)	TET2, TET2-AS1 (V895I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 2904015	NM_001127208.3(TET2):c.3081C>T (p.Thr1027=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2903592	NM_001127208.3(TET2):c.5077T>A (p.Tyr1693Asn)	TET2, TET2-AS1 (Y1693N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2903323	NM_001127208.3(TET2):c.3813C>T (p.Cys1271=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2901244	NM_001127208.3(TET2):c.3381A>G (p.Gln1127=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2900855	NM_001127208.3(TET2):c.1489A>T (p.Thr497Ser)	TET2, TET2-AS1 (T497S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 2899053	NM_001127208.3(TET2):c.1741C>T (p.Arg581Cys)	TET2, TET2-AS1 (R581C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2898264	NM_001127208.3(TET2):c.5898T>C (p.Arg1966=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2898263	NM_001127208.3(TET2):c.5802G>A (p.Lys1934=)	TET2, TET2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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