Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | PBRM1 |
Variant | Q1480Tfs*29 |
Impact List | frameshift |
Protein Effect | unknown |
Gene Variant Descriptions | PBRM1 Q1480Tfs*29 indicates a shift in the reading frame starting at amino acid 1480 and terminating 29 residues downstream causing a premature truncation of the 1689 amino acid Pbrm1 protein (UniProt.org). Q1480Tfs*29 has not been characterized in the scientific literature and therefore, its effect on Pbrm1 protein function is unknown (PubMed, Jul 2024). |
Associated Drug Resistance | |
Category Variants Paths |
PBRM1 mutant PBRM1 Q1480Tfs*29 |
Transcript | NM_018313.5 |
gDNA | chr3:g.52550560dupT |
cDNA | c.4437dupA |
Protein | p.Q1480Tfs*29 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001394876.1 | chr3:g.52550556_52550557insTTGT | c.4437_4438insACAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001400484.1 | chr3:g.(52550551_52550749) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405552.1 | chr3:g.(52558277_52558366) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_018313.4 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001366073.2 | chr3:g.52550613_52550614insTTTGT | c.4437_4438insACAAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405558.1 | chr3:g.(52550551_52550749) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001400501.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
XM_017006731.2 | chr3:g.(52558301_52558390) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
XM_017006730.2 | chr3:g.(52558301_52558390) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405626.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
XM_024453619.2 | chr3:g.(52558274_52558363) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405565.1 | chr3:g.(52550551_52550749) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_181042.4 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405577.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405624.1 | chr3:g.52550556_52550557insTTGT | c.4437_4438insACAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405640.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_181042.5 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001394877.1 | chr3:g.52550556_52550557insTTGT | c.4437_4438insACAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001400500.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001394875.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405555.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405570.1 | chr3:g.52558270_52558271insTTGGGGGGGGGGT | c.4437_4438insACCCCCCCCCCAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405633.1 | chr3:g.(52550551_52550749) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001366074.2 | chr3:g.52550610_52550611insTTTGGGGT | c.4437_4438insACCCCAAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405635.1 | chr3:g.(52550551_52550749) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
XM_017006734.3 | chr3:g.(52558271_52558360) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405593.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
XM_047448445.1 | chr3:g.(52558298_52558387) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
XM_047448444.1 | chr3:g.(52558298_52558387) | c.(4438_4527) | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405627.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001405563.1 | chr3:g.52550556_52550557insTTGT | c.4437_4438insACAA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_018313.5 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
NM_001400496.1 | chr3:g.52550560dupT | c.4437dupA | p.Q1480Tfs*29 | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
PBRM1 Q1480Tfs*29 | unknown |