Gene Variant Detail

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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

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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_001126115.2 chr17:g.7673801_7673806delACGCAC c.420_425delGCGTGT p.R141_V142delRV RefSeq GRCh38/hg38
NM_001126117.1 chr17:g.7673801_7673806delACGCAC c.420_425delGCGTGT p.R141_V142delRV RefSeq GRCh38/hg38
NM_000546 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001126112 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001126115.1 chr17:g.7673801_7673806delACGCAC c.420_425delGCGTGT p.R141_V142delRV RefSeq GRCh38/hg38
NM_001126118.2 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001126118.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276697.1 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_001407266.1 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001407267.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276696.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276761.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276696 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_001126113 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001126117.2 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_001126116.2 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_001407268.1 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001276697.3 chr17:g.7673720_7673725delGGGCAG c.419_424delTGCCCC p.L140_P141delLP RefSeq GRCh38/hg38
NM_001126118 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276698.3 chr17:g.7673720_7673725delGGGCAG c.419_424delTGCCCC p.L140_P141delLP RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001126117 chr17:g.7673801_7673806delACGCAC c.420_425delGCGTGT p.R141_V142delRV RefSeq GRCh38/hg38
NM_001276760.1 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_001276696.3 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001407270.1 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_001126115 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_001126116 chr17:g.7673801_7673806delACGCAC c.420_425delGCGTGT p.R141_V142delRV RefSeq GRCh38/hg38
NM_001276761.3 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276695.3 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_001407271.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276695.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276760 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001407265.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001407263.1 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276760.3 chr17:g.7675072_7675077delCTCATG c.419_424delATGAGC p.H140_E141delHE RefSeq GRCh38/hg38
NM_001276699.3 chr17:g.7673720_7673725delGGGCAG c.419_424delTGCCCC p.L140_P141delLP RefSeq GRCh38/hg38
NM_001276698 chr17:g.7673720_7673725delGGGCAG c.419_424delTGCCCC p.L140_P141delLP RefSeq GRCh38/hg38
NM_001276699 chr17:g.7673720_7673725delGGGCAG c.419_424delTGCCCC p.L140_P141delLP RefSeq GRCh38/hg38
NM_001276761 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_001126114.2 chr17:g.7675189_7675194delGCAGGT c.418_423delACCTGC p.T140_C141delTC RefSeq GRCh38/hg38
NM_001126112.2 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_001276695 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

Filtering

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  • 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")

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References