Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | TSC2 |
Variant | L369P |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TSC2 L369P lies within the TSC1-interacting region of the Tsc2 protein (UniProt.org). L369P fails to inhibit mTorc1 activity as indicated by reduced inhibition of S6k phosphorylation and results in decreased binding to Tsc1 in cultured cells (PMID: 31799751). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 L369P |
Transcript | NM_000548.5 |
gDNA | chr16:g.2060800T>C |
cDNA | c.1106T>C |
Protein | p.L369P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005255531.4 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001114382.3 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001406663.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_005255529.4 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001363528.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522637.3 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001406665.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_017023615.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522639.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_024450413.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_021055.3 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_017023616.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522636.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522639.3 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001406664.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522640.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522637.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001077183.3 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001114382.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001077183.2 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001370404.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
XM_011522636.3 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
NM_001406677.1 | chr16:g.2061913_2061914delTTinsCC | c.1105_1106delTTinsCC | p.L369P | RefSeq | GRCh38/hg38 |
NM_001370405.1 | chr16:g.2060800T>C | c.1106T>C | p.L369P | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|