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Gene | TP53 |
Variant | R213G |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TP53 R213G lies within the DNA-binding domain of the Tp53 protein (PMID: 15510160). R213G has been identified in sequencing studies (PMID: 28744014, PMID: 26319365, PMID: 31590326), but has not been biochemically characterized and therefore, its effect on Tp53 protein function is unknown (PubMed, Feb 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon6 TP53 R213G |
Transcript | NM_000546.6 |
gDNA | chr17:g.7674894G>C |
cDNA | c.637C>G |
Protein | p.R213G |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001407270.1 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7674894G>C | c.637C>G | p.R213G | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
TP53 R213G | unknown |