Gene Variant Detail

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Gene CDK12
Variant V919F
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CDK12 V919F lies within the protein kinase domain of the Cdk12 protein (UniProt.org). V919F has been identified in sequencing studies (PMID: 26787835), but has not been biochemically characterized and therefore, its effect on Cdk12 protein function is unknown (PubMed, Jan 2024).
Associated Drug Resistance
Category Variants Paths

CDK12 mutant CDK12 V919F

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Transcript NM_016507.4
gDNA chr17:g.39511617G>T
cDNA c.2755G>T
Protein p.V919F
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011524892 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436278.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024752 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436268.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524905.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024745 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524898 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524902 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436273.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024748 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524906 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524894.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436261.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524900 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024748.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524898.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436272.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524903.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524906.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524907 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436269.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024747 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436256.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436259.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524896 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436266.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024749 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436274.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436260.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436255.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524895.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024750.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524903 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524907.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
NM_016507.4 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024747.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524898.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436277.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524897 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436293.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024752.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
NM_015083.4 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024751 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524906.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
NM_015083.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524897.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524892.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_024450801.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436267.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
NM_016507 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024751.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524893.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524907.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524895 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024749.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524897.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524900.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524893 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024750 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524899.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
NM_016507.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436265.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436257.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524901.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024746 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524902.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524894 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524893.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436258.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436287.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436289.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524901 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524899 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_005257458.4 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524895.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
NM_015083 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436275.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_017024744 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436270.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_005257458 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436288.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524894.3 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524905 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_011524896.2 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436276.1 chr17:g.39511617G>T c.2755G>T p.V919F RefSeq GRCh38/hg38
XM_047436279.1 chr17:g.39511617G>T c.2755G>T p.V919F 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