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Gene | TP53 |
Variant | Q136L |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TP53 Q136L lies within the DNA-binding domain and CCAR2, HIPK1, ZNF385A, FBXO42, and AXIN1-interacting regions of the Tp53 protein (UniProt.org). Q136L has been identified in sequencing studies (PMID: 25401301, PMID: 22493262), but has not been biochemically characterized and therefore, its effect on Tp53 protein function is unknown (PubMed, Feb 2025). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon5 TP53 Q136L |
Transcript | NM_000546.6 |
gDNA | chr17:g.7675205T>A |
cDNA | c.407A>T |
Protein | p.Q136L |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001126113 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7675205T>A | c.407A>T | p.Q136L | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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