Gene Variant Detail

Contact

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 DNMT3A
Variant F414S
Impact List missense
Protein Effect unknown
Gene Variant Descriptions DNMT3A F414S does not lie within any known functional domains of the Dnmt3a protein (UniProt.org). F414S has been identified in sequencing studies (PMID: 21720365), but has not been biochemically characterized and therefore, its effect on Dnmt3a protein function is unknown (PubMed, Oct 2024).
Associated Drug Resistance
Category Variants Paths

DNMT3A mutant DNMT3A F414S

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.

Transcript NM_022552.5
gDNA chr2:g.25246658A>G
cDNA c.1241T>C
Protein p.F414S
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_175629 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_017003526.1 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_017003526.2 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_017003526 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_005264175.6 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
NM_022552.5 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_005264175.5 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_011532664.2 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
NM_022552 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_011532664 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
NM_022552.4 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
NM_175629.2 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_005264175 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
NM_175629.2 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_011532664.3 chr2:g.25246658A>G c.1241T>C p.F414S RefSeq GRCh38/hg38
XM_047443593.1 chr2:g.25246658A>G c.1241T>C p.F414S 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