"Ambry Genetics"[submitter] AND "TET2"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2476927	NM_001127208.3(TET2):c.410G>C (p.Ser137Thr)	TET2, TET2-AS1 (S137T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1910894	NM_001127208.3(TET2):c.418A>G (p.Asn140Asp)	TET2, TET2-AS1 (N140D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2474774	NM_001127208.3(TET2):c.435T>G (p.Ser145Arg)	TET2, TET2-AS1 (S145R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1915496	NM_001127208.3(TET2):c.478G>A (p.Val160Ile)	TET2, TET2-AS1 (V160I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2404452	NM_001127208.3(TET2):c.528T>A (p.Asn176Lys)	TET2, TET2-AS1 (N176K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2363063	NM_001127208.3(TET2):c.917A>G (p.Lys306Arg)	TET2, TET2-AS1 (K306R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176232	NM_001127208.3(TET2):c.1091G>A (p.Gly364Asp)	TET2, TET2-AS1 (G364D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2189134	NM_001127208.3(TET2):c.1331C>T (p.Thr444Ile)	TET2, TET2-AS1 (T444I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2303718	NM_001127208.3(TET2):c.1496C>T (p.Pro499Leu)	TET2, TET2-AS1 (P499L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325501	NM_001127208.3(TET2):c.1531C>T (p.His511Tyr)	TET2, TET2-AS1 (H511Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317994	NM_001127208.3(TET2):c.1625A>C (p.Lys542Thr)	TET2, TET2-AS1 (K542T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279085	NM_001127208.3(TET2):c.1765A>G (p.Ile589Val)	TET2, TET2-AS1 (I589V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1982714	NM_001127208.3(TET2):c.1904A>G (p.Gln635Arg)	TET2, TET2-AS1 (Q635R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3176233	NM_001127208.3(TET2):c.2039G>T (p.Arg680Ile)	TET2, TET2-AS1 (R680I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325502	NM_001127208.3(TET2):c.2266A>C (p.Ile756Leu)	TET2, TET2-AS1 (I756L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176234	NM_001127208.3(TET2):c.2518C>G (p.Leu840Val)	TET2, TET2-AS1 (L840V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266158	NM_001127208.3(TET2):c.2716A>G (p.Met906Val)	TET2, TET2-AS1 (M906V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176235	NM_001127208.3(TET2):c.2728C>A (p.Gln910Lys)	TET2, TET2-AS1 (Q910K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258257	NM_001127208.3(TET2):c.2763A>G (p.Ile921Met)	TET2, TET2-AS1 (I921M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2281072	NM_001127208.3(TET2):c.2996A>C (p.Glu999Ala)	TET2, TET2-AS1 (E999A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176236	NM_001127208.3(TET2):c.3077A>C (p.Glu1026Ala)	TET2, TET2-AS1 (E1026A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1909591	NM_001127208.3(TET2):c.3084G>A (p.Met1028Ile)	TET2, TET2-AS1 (M1028I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2220094	NM_001127208.3(TET2):c.3269A>G (p.Lys1090Arg)	TET2, TET2-AS1 (K1090R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220853	NM_001127208.3(TET2):c.3326C>T (p.Ser1109Phe)	TET2, TET2-AS1 (S1109F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2258778	NM_001127208.3(TET2):c.4289G>A (p.Gly1430Glu)	TET2, TET2-AS1 (G1430E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341433	NM_001127208.3(TET2):c.4793A>G (p.Tyr1598Cys)	TET2, TET2-AS1 (Y1598C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27