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Gene | TET2 |
Variant | P174H |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TET2 P174H does not lie within any known functional domains of the Tet2 protein (UniProt.org). P174H has been identified in sequencing studies (PMID: 26415585), but has not been biochemically characterized and therefore, its effect on Tet2 protein function is unknown (PubMed, Oct 2022). |
Associated Drug Resistance | |
Category Variants Paths |
TET2 mutant TET2 P174H |
Transcript | NM_001127208.3 |
gDNA | chr4:g.105234463C>A |
cDNA | c.521C>A |
Protein | p.P174H |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017008319.2 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_024454103.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_006714242.3 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
NM_001127208.3 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_005263082.3 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_047415840.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_047415839.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_024454102.2 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_024454102.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_047415843.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
NM_017628 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_006714242 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_005263082.4 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_047415842.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_005263082 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
NM_017628.4 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_017008319.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_047415841.1 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
NM_001127208 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_024454103.2 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
NM_001127208.2 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
NM_017628.4 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_006714242.4 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
XM_017008319 | chr4:g.105234463C>A | c.521C>A | p.P174H | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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