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Gene FANCL
Variant A51T
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FANCL A51T does not lie within any known functional domains of the Fancl protein (UniProt.org). A51T has not been characterized in the scientific literature and therefore, its effect on Fancl protein function is unknown (PubMed, Feb 2024).
Associated Drug Resistance
Category Variants Paths

FANCL mutant FANCL A51T

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Transcript NM_018062.4
gDNA chr2:g.58232058C>T
cDNA c.151G>A
Protein p.A51T
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001410792.1 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_017004415 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532940.4 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532942 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532941.2 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_018062.3 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_018062.4 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532939 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532941 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_017004415.2 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_018062 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_047444852.1 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_005264395 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_005264395.5 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532939.4 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_001374615.1 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532940 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532940.3 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_017004414.2 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_017004414 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_047444853.1 chr2:g.58165820C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532942.3 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_001114636.1 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532942.4 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_001114636.1 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
NM_001114636 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_047444854.1 chr2:g.58165820C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_011532939.3 chr2:g.58232058C>T c.151G>A p.A51T RefSeq GRCh38/hg38
XM_005264395.4 chr2:g.58232058C>T c.151G>A p.A51T 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 Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References