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Gene | TSC2 |
Variant | R1745H |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TSC2 R1745H lies within the Rap-GAP domain of the Tsc2 protein (UniProt.org). R1745H has been identified in sequencing studies (PMID: 35300216, PMID: 37994105), but has not been biochemically characterized and therefore, its effect on Tsc2 protein function is unknown (PubMed, Sep 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 R1745H |
Transcript | NM_000548.5 |
gDNA | chr16:g.2088300G>A |
cDNA | c.5234G>A |
Protein | p.R1745H |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000548.4 | chr16:g.2088300G>A | c.5234G>A | p.R1745H | RefSeq | GRCh38/hg38 |
NM_000548 | chr16:g.2088300G>A | c.5234G>A | p.R1745H | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2088300G>A | c.5234G>A | p.R1745H | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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