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Gene TSC2
Variant A1141T
Impact List missense
Protein Effect unknown
Gene Variant Descriptions TSC2 A1141T does not lie within any known functional domains of the Tsc2 protein (UniProt.org). A1141T has been identified in sequencing studies (PMID: 25724664), but has not been biochemically characterized and therefore, its effect on Tsc2 protein function is unknown (PubMed, Oct 2024).
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 A1141T

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Transcript NM_000548.5
gDNA chr16:g.2080188G>A
cDNA c.3421G>A
Protein p.A1141T
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011522640 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_005255531 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001077183 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522639 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001077183.2 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001406665.1 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522639.3 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001370405.1 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_000548.5 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_005255529.4 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522636 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001363528.2 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_021055.3 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_005255531.4 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_017023616 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522640.2 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001370404.1 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_000548.4 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001114382 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001077183.3 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001406698.1 chr16:g.2088290G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_001406679.1 chr16:g.2081684G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_005255529 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
NM_000548 chr16:g.2080188G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_017023616.1 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_024450413.1 chr16:g.2080320G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38
XM_011522639.2 chr16:g.2080317G>A c.3421G>A p.A1141T RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries