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| Gene | BRIP1 |
| Variant | T997Rfs*61 |
| Impact List | frameshift |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | BRIP1 T997Rfs*61 indicates a shift in the reading frame starting at amino acid 997 and terminating 61 residues downstream causing a premature truncation of the 1249 amino acid Brip1 protein (UniProt.org). T997Rfs*61 has not been characterized, however, due to the effects of other truncation mutations downstream of T997 (PMID: 18628483), is predicted to lead to a loss of Brip1 protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
BRIP1 mutant BRIP1 inact mut BRIP1 T997fs BRIP1 T997Rfs*61 |
| Transcript | NM_032043.3 |
| gDNA | chr17:g.61684063_61684066delTGTT |
| cDNA | c.2990_2993delCAAA |
| Protein | p.T997Rfs*61 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_011525335.4 | chr17:g.61684063_61684066delTGTT | c.2990_2993delCAAA | p.T997Rfs*61 | RefSeq | GRCh38/hg38 |
| NM_032043.3 | chr17:g.61684063_61684066delTGTT | c.2990_2993delCAAA | p.T997Rfs*61 | RefSeq | GRCh38/hg38 |
| XM_047436892.1 | chr17:g.61684063_61684066delTGTT | c.2990_2993delCAAA | p.T997Rfs*61 | RefSeq | GRCh38/hg38 |
| XM_047436891.1 | chr17:g.61684063_61684066delTGTT | c.2990_2993delCAAA | p.T997Rfs*61 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| BRIP1 T997Rfs*61 | loss of function - predicted |