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Gene | CDK12 |
Variant | R858W |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CDK12 R858W lies within the protein kinase domain of the Cdk12 protein (PMID: 22512864). R858W has been identified in the scientific literature (PMID: 30487607, PMID: 39321214, PMID: 35487690), but has not been biochemically characterized and therefore, its effect on Cdk12 protein function is unknown (PubMed, Jun 2025). |
Associated Drug Resistance | |
Category Variants Paths |
CDK12 mutant CDK12 R858W |
Transcript | NM_016507.4 |
gDNA | chr17:g.39501402C>T |
cDNA | c.2572C>T |
Protein | p.R858W |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_015083 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
NM_015083.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
NM_015083.4 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
NM_016507 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
NM_016507.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
NM_016507.4 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_005257458 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_005257458.4 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524892 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524892.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524893 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524893.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524893.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524894 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524894.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524894.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524895 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524895.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524895.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524896 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524896.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524897 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524897.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524897.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524898 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524898.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524898.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524899 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524899.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524900 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524900.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524901 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524901.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524902 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524902.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524903 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524903.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524905 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524905.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524906 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524906.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524906.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524907 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524907.2 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_011524907.3 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024744 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024745 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024746 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024747 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024747.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024748 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024748.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024749 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024749.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024750 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024750.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024751 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024751.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024752 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_017024752.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_024450801.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436255.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436256.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436257.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436258.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436259.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436260.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436261.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436265.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436266.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436267.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436268.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436269.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436270.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436272.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436273.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436274.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436275.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436276.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436277.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436278.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436279.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436287.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436288.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436289.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
XM_047436293.1 | chr17:g.39501402C>T | c.2572C>T | p.R858W | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
CDK12 R858W | prostate cancer | decreased response | Rucaparib | Preclinical - Cell culture | Actionable | In a preclinical study, expression of CDK12 R858W in CDK12 knockout prostate cancer cell lines demonstrated reduced sensitivity to Rubraca (rucaparib) compared cells with the CDK12 knockout alone in culture (PMID: 39321214). | 39321214 |
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