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Gene | CDK12 |
Variant | E1327D |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CDK12 E1327D does not lie within any known functional domains of the Cdk12 protein (UniProt.org). E1327D 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 E1327D |
Transcript | NM_016507.4 |
gDNA | chr17:g.39530824G>C |
cDNA | c.3981G>C |
Protein | p.E1327D |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017024749.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436259.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524899 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436256.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524903 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524901.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024744 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524897.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
NM_016507.4 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524900 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524893.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024745 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524899.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024747 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524906 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524896.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524894 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524895.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024746 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524901 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024747.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524898.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524896 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524897.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524902.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524895.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524906.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524897 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
NM_016507.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024748 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524906.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
NM_016507 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436261.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524903.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524894.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436260.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_024450801.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524900.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524893.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524898.3 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524894.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524902 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524905.2 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436258.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024748.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524895 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524898 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436257.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_047436255.1 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_017024749 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524905 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
XM_011524893 | chr17:g.39530824G>C | c.3981G>C | p.E1327D | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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