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Gene | TP53 |
Variant | T140_C141del |
Impact List | deletion |
Protein Effect | unknown |
Gene Variant Descriptions | TP53 T140_C141del results in the deletion of two amino acids in the DNA-binding domain of the Tp53 protein from amino acids 140 to 141 (PMID: 22713868). T140_C141del has not been characterized and therefore, its effect on Tp53 protein function is unknown (PubMed, Jun 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon5 TP53 T140_C141del |
Transcript | NM_000546.6 |
gDNA | chr17:g.7675189_7675194delGCAGGT |
cDNA | c.418_423delACCTGC |
Protein | p.T140_C141delTC |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001276695.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126117 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001276697 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001126115.1 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276761.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126117.2 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001276699.3 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001276697.1 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276695.3 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001276761 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126117.1 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276761.3 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126116 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276696.3 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001407269.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001276698.1 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001126118.2 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126115 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001276760.3 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001407267.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001276699 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001126116.2 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001126115.2 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001276760 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001126116.1 | chr17:g.7673801_7673806delACGCAC | c.420_425delGCGTGT | p.R141_V142delRV | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276696 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276696.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126118.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001407263.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276760.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276695 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001126118 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001407271.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
NM_001276698 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001276699.1 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001407265.1 | chr17:g.7675072_7675077delCTCATG | c.419_424delATGAGC | p.H140_E141delHE | RefSeq | GRCh38/hg38 |
NM_001276697.3 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_001276698.3 | chr17:g.7673720_7673725delGGGCAG | c.419_424delTGCCCC | p.L140_P141delLP | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7675189_7675194delGCAGGT | c.418_423delACCTGC | p.T140_C141delTC | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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