Gene Variant Detail

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Gene CDK12
Variant R779C
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CDK12 R779C lies within the protein kinase domain of the Cdk12 protein (PMID: 22512864). R779C has not been characterized in the scientific literature and therefore, its effect on Cdk12 protein function is unknown (PubMed, Oct 2023).
Associated Drug Resistance
Category Variants Paths

CDK12 mutant CDK12 R779C

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Transcript NM_016507.4
gDNA chr17:g.39494610C>T
cDNA c.2335C>T
Protein p.R779C
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011524905 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524893 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524906.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024744 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436278.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436275.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524892.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524900 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024746 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524907 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436274.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524895.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524899 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_005257458.4 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436260.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436272.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024750.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
NM_016507.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024751.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436259.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524907.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436268.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524901 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_024450801.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436279.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524900.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436257.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024748 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524896.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436289.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524897 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436277.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024752 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524894 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524901.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436287.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524895 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024749 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524898.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524894.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436266.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524906.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524903.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436265.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436276.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
NM_015083.4 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024745 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436255.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436261.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_005257458 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524893.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024750 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436267.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524892 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524894.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
NM_015083 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524893.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024747 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024751 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
NM_015083.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524896 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436256.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436273.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524897.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436269.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524902.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524907.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524906 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524899.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524895.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524903 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524905.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024747.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436270.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436288.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436258.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524897.2 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024748.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524898.3 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024752.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
NM_016507 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
NM_016507.4 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_047436293.1 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524902 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_011524898 chr17:g.39494610C>T c.2335C>T p.R779C RefSeq GRCh38/hg38
XM_017024749.1 chr17:g.39494610C>T c.2335C>T p.R779C 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