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Gene | TET2 |
Variant | R506* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TET2 R506* results in a premature truncation of the Tet2 protein at amino acid 506 of 2002 (UniProt.org). R506* results in a loss of 5-hydroxymethylcytosine (5hmc) formation in cultured cells (PMID: 24994606), and therefore, is predicted to lead to a loss of Tet2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TET2 mutant TET2 inact mut TET2 R506* |
Transcript | NM_001127208.3 |
gDNA | chr4:g.105235458A>T |
cDNA | c.1516A>T |
Protein | p.R506* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_024454103.2 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_005263082 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_024454102.2 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_047415839.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
NM_001127208 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_047415840.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_047415843.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_005263082.4 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_047415841.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
NM_001127208.2 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_006714242 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_024454102.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
NM_017628 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
NM_001127208.3 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_005263082.3 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_006714242.3 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_017008319.2 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_017008319 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_024454103.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_006714242.4 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
NM_017628.4 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_047415842.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
XM_017008319.1 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
NM_017628.4 | chr4:g.105235458A>T | c.1516A>T | p.R506* | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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