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Gene | TET2 |
Variant | Q891fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TET2 Q891fs results in a change in the amino acid sequence of the Tet2 protein beginning at aa 891 of 2002, likely resulting in premature truncation of the functional protein (UniProt.org). Q891fs has not been characterized however, due to the effects of other truncation mutations downstream of Q891 (PMID: 24994606), is predicted to lead to a loss of Tet2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TET2 mutant TET2 inact mut TET2 Q891fs |
Transcript | NM_001127208.3 |
gDNA | chr4:g.(105236612_105236613) |
cDNA | c.(2671_2670) |
Protein | p.Q891fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_017628.4 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_006714242.4 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
NM_001127208.3 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_047415841.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_017008319.2 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
NM_017628.4 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_047415840.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_017008319.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
NM_001127208.2 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_024454102.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_047415839.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_024454103.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_006714242.3 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_005263082.4 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_047415843.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_024454103.2 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_005263082.3 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_024454102.2 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
XM_047415842.1 | chr4:g.(105236612_105236613) | c.(2671_2670) | p.Q891fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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