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Gene TSC2
Variant L688M
Impact List missense
Protein Effect unknown
Gene Variant Descriptions TSC2 L688M does not lie within any known functional domains of the Tsc2 protein (UniProt.org). L688M has been identified in sequencing studies (PMID: 30503610), but has not been biochemically characterized and therefore, its effect on Tsc2 protein function is unknown (PubMed, Jul 2024).
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 L688M

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Transcript NM_000548.5
gDNA chr16:g.2071899C>A
cDNA c.2062C>A
Protein p.L688M
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017023615 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_024450413.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001077183.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522639.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406685.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001318831 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_017023615.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_017023616 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406683.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522636 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522637 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001114382 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001077183 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406679.1 chr16:g.2072352_2072354delCTCinsATG c.2062_2064delCTCinsATG p.L688M RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001077183.3 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406675.1 chr16:g.2072352_2072354delCTCinsATG c.2062_2064delCTCinsATG p.L688M RefSeq GRCh38/hg38
NM_001318829.1 chr16:g.2072352_2072354delCTCinsATG c.2062_2064delCTCinsATG p.L688M RefSeq GRCh38/hg38
NM_001406684.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_000548 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001318829.2 chr16:g.2072352_2072354delCTCinsATG c.2062_2064delCTCinsATG p.L688M RefSeq GRCh38/hg38
XM_005255529 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406664.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406686.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001370405.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406698.1 chr16:g.2081780C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001318829 chr16:g.2072352_2072354delCTCinsATG c.2062_2064delCTCinsATG p.L688M RefSeq GRCh38/hg38
XM_011522640 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522637.3 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522637.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_017023616.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406663.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522639.3 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406688.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001363528.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406676.1 chr16:g.2072352_2072354delCTCinsATG c.2062_2064delCTCinsATG p.L688M RefSeq GRCh38/hg38
NM_000548.4 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001318831.2 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406687.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_005255531 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_005255529.4 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_021055.3 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406682.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522640.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406665.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001318831.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_000548.5 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001370404.1 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_005255531.4 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
XM_011522639 chr16:g.2071899C>A c.2062C>A p.L688M RefSeq GRCh38/hg38
NM_001406680.1 chr16:g.2076090C>A c.2062C>A p.L688M RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • 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
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Molecular Profile Protein Effect Treatment Approaches
TSC2 L688M unknown