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Gene | TSC2 |
Variant | Q572H |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TSC2 Q572H does not lie within any known functional domains of the Tsc2 protein (UniProt.org). Q572H has not been characterized in the scientific literature and therefore, its effect on Tsc2 protein function is unknown (PubMed, Sep 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 Q572H |
Transcript | NM_000548.5 |
gDNA | chr16:g.2065635G>T |
cDNA | c.1716G>T |
Protein | p.Q572H |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001077183.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522640.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_005255529 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001370404.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522636.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_000548 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_005255529.4 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001114382 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522637 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522639 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_017023616.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522639.3 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_017023615.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001406665.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522636.3 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001077183 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_005255531 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_024450413.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001406663.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522639.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_017023615 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522636 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001370405.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522640 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_005255531.4 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001077183.3 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522637.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_021055.3 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_017023616 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001114382.3 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001406664.1 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001363528.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
XM_011522637.3 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
NM_001114382.2 | chr16:g.2065635G>T | c.1716G>T | p.Q572H | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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