Gene Variant Detail

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Gene CDK12
Variant H999Y
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CDK12 H999Y lies within the protein kinase domain of the Cdk12 protein (PMID: 22512864). H999Y has not been characterized in the scientific literature and therefore, its effect on Cdk12 protein function is unknown (PubMed, Apr 2024).
Associated Drug Resistance
Category Variants Paths

CDK12 mutant CDK12 H999Y

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Transcript NM_016507.4
gDNA chr17:g.39519987C>T
cDNA c.2995C>T
Protein p.H999Y
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017024751.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436256.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024749.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524907 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024744 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024745 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436273.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
NM_015083.4 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_005257458.4 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024747 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436267.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524903.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524900.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_005257458 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436288.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436289.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
NM_016507 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524893 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524893.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524899.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436265.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524901 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436268.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436257.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524906.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524895.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524894.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524896 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524901.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524905 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436274.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524893.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436287.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024748 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524900 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436277.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024752 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_024450801.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024750.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524906 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024748.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524894.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024751 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436270.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024749 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436255.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524895.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436279.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436260.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524898.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436269.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436258.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024746 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524896.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524899 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524905.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524897.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
NM_016507.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524902 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436276.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524898 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436275.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
NM_015083 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524895 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524907.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524906.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024750 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436272.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524903 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436278.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436266.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436259.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524894 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024747.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524907.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
NM_016507.4 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_017024752.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524897.3 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524898.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524902.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_047436261.1 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
NM_015083.2 chr17:g.39519987C>T c.2995C>T p.H999Y RefSeq GRCh38/hg38
XM_011524897 chr17:g.39519987C>T c.2995C>T p.H999Y 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