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Gene | TSC2 |
Variant | R905fs |
Impact List | frameshift |
Protein Effect | loss of function |
Gene Variant Descriptions | TSC2 R905fs results in a change in the amino acid sequence of the Tsc2 protein beginning at aa 905 of 1807, likely resulting in premature truncation of the functional protein (UniProt.org). R905fs confers a loss of function to the Tsc2 protein as indicated by increased p62 expression associated with decreased autophagy, and reduced ciliogenesis in patient samples (PMID: 29937275). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 R905fs |
Transcript | NM_000548.5 |
gDNA | chr16:g.(2076140_2076141) |
cDNA | c.(2713_2712) |
Protein | p.R905fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001077183 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001406664.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522637.3 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_017023615.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522640 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_021055.3 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_017023616.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001114382 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522637.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001114382.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522636.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001114382.3 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_000548 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_024450413.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001370404.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_017023616 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001077183.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_005255529 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001406665.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_017023615 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522636.3 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522639 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_005255529.4 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522640.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_005255531.4 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001077183.3 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522636 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_005255531 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001370405.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522637 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_017023618.1 | chr16:g.(2083813_2083814) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001363528.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522639.2 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
XM_011522639.3 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
NM_001406663.1 | chr16:g.(2076140_2076141) | c.(2713_2712) | p.R905fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
TSC2 R905fs | loss of function | mTOR Inhibitor mTORC1 Inhibitor |