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Gene | PBRM1 |
Variant | R761G |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | PBRM1 R761G does not lie within any known functional domains of the Pbrm1 protein (UniProt.org). R761G has not been characterized in the scientific literature and therefore, its effect on Pbrm1 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
PBRM1 mutant PBRM1 R761G |
Transcript | NM_018313.5 |
gDNA | chr3:g.52609599T>C |
cDNA | c.2281A>G |
Protein | p.R761G |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001400475.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405565.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400504.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405629.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405557.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394877.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405594.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405583.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405643.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394876.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405640.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_018313.4 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400470.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405561.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405639.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001366076.2 | chr3:g.52609602G>C | c.2281C>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405581.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405634.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_181042.4 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001350075.2 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400501.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405603.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405632.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405592.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405593.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405626.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394871.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400474.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405623.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
XM_017006750.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394867.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405611.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400500.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405610.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394868.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001350075.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405575.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405556.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405628.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405563.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394869.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405585.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400473.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405590.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405641.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405555.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405624.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400479.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394874.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405558.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405633.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405631.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405605.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405627.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405635.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405589.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_181042.5 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405609.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405570.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
XM_017006749.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394875.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400490.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405576.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
XM_017006748.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400496.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405630.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_018313.5 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400484.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405559.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394873.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405567.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001400481.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405612.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001394872.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
XM_047448462.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405578.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
XM_017006758.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405577.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405584.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405579.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
NM_001405588.1 | chr3:g.52609599T>C | c.2281A>G | p.R761G | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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