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 Q606*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions DNMT3A Q606* results in a premature truncation of the Dnmt3a protein at amino acid 606 of 912 (UniProt.org). Q606* has not been characterized, however, due to the effects of other truncation mutations downstream of Q606 (PMID: 28872462, PMID: 26595813, PMID: 35639959), is predicted to lead to a loss of Dnmt3a protein function.
Associated Drug Resistance
Category Variants Paths

DNMT3A mutant DNMT3A inact mut DNMT3A Q606*

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.25244190G>A
cDNA c.1816C>T
Protein p.Q606*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_022552 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
NM_175629 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_005264175 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
NM_022552.5 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_017003526 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_011532664 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
NM_175629.2 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
NM_022552.4 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_005264175.5 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
NM_175629.2 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_005264175.6 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_011532664.3 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_017003526.1 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_047443593.1 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_011532664.2 chr2:g.25244190G>A c.1816C>T p.Q606* RefSeq GRCh38/hg38
XM_017003526.2 chr2:g.25244190G>A c.1816C>T p.Q606* 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