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Gene | TSC2 |
Variant | N1064Kfs*104 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TSC2 N1064Kfs*104 indicates a shift in the reading frame starting at amino acid 1064 and terminating 104 residues downstream causing a premature truncation of the 1807 amino acid Tsc2 protein (UniProt.org). N1064Kfs*104 has not been characterized however, due to the effects of other truncation mutations downstream of N1064 (PMID: 22903760), is predicted to lead to a loss of Tsc2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 N1064Kfs*104 |
Transcript | NM_000548.5 |
gDNA | chr16:g.2079335dupA |
cDNA | c.3191dupA |
Protein | p.N1064Kfs*104 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000548.4 | chr16:g.2079335dupA | c.3191dupA | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
NM_001406691.1 | chr16:g.(2086196_2086862) | c.(3190_3504) | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
XM_011522636.2 | chr16:g.2079335dupA | c.3191dupA | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
NM_001114382.3 | chr16:g.2079335dupA | c.3191dupA | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
NM_001114382.2 | chr16:g.2079335dupA | c.3191dupA | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
XM_011522636.3 | chr16:g.2079335dupA | c.3191dupA | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2079335dupA | c.3191dupA | p.N1064Kfs*104 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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