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Gene | RB1 |
Variant | K319Nfs*13 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | RB1 K319Nfs*13 indicates a shift in the reading frame starting at amino acid 319 and terminating 13 residues downstream causing a premature truncation of the 928 amino acid Rb1 protein (UniProt.org). Due to the loss of all known functional domains (UniProt.org), K319Nfs*13 is predicted to lead to a loss of Rb1 function. |
Associated Drug Resistance | |
Category Variants Paths |
RB1 mutant RB1 inact mut RB1 K319Nfs*13 |
Transcript | NM_000321.3 |
gDNA | chr13:g.48367511delA |
cDNA | c.957delA |
Protein | p.K319Nfs*13 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000321.2 | chr13:g.48367511delA | c.957delA | p.K319Nfs*13 | RefSeq | GRCh38/hg38 |
NM_001407165.1 | chr13:g.48367511delA | c.957delA | p.K319Nfs*13 | RefSeq | GRCh38/hg38 |
NM_000321.3 | chr13:g.48367511delA | c.957delA | p.K319Nfs*13 | RefSeq | GRCh38/hg38 |
NM_000321 | chr13:g.48367508delT | c.954delT | p.K319Nfs*13 | RefSeq | GRCh38/hg38 |
NM_001407166.1 | chr13:g.48367511delA | c.957delA | p.K319Nfs*13 | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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