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Gene | BRAF |
Variant | V47_M438del |
Impact List | deletion |
Protein Effect | gain of function - predicted |
Gene Variant Descriptions | BRAF V47_M438del results in the deletion of 392 amino acids of the Braf protein from amino acids 47 to 438 (UniProt.org). V47_M438del (reported as internal deletion of exons 2-10) has been associated with acquired resistance to a Braf inhibitor in a patient (PMID: 32669268), and is predicted to lead to a gain of Braf protein function due to the deletion of the CR1 autoinhibitory domain and preservation of the protein kinase domain (PMID: 23890088, PMID: 22113612, PMID: 29171936). |
Associated Drug Resistance | Y |
Category Variants Paths |
BRAF mutant BRAF act mut BRAF V47_M438del |
Transcript | NM_004333.6 |
gDNA | chr7:g.140783022_140850213del67192 |
cDNA | c.141_1314+2del67192 |
Protein | p.V47_M438del392 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047420769.1 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
NM_001378471.1 | chr7:g.140781585_140850214del68630 | c.139_1314del68630 | p.V47_K438del392 | RefSeq | GRCh38/hg38 |
NM_001378470.1 | chr7:g.140781592_140834872del53281 | c.139_1314del53281 | p.A47_Y438del392 | RefSeq | GRCh38/hg38 |
XM_005250045 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
NM_001378469.1 | chr7:g.140781628_140850212del68585 | c.139_1314del68585 | p.V47_G438del392 | RefSeq | GRCh38/hg38 |
NM_001354609.1 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
XM_017012558.1 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
XM_047420770.1 | chr7:g.140739911_140800369del60459 | c.139_1314del60459 | p.S47_P438del392 | RefSeq | GRCh38/hg38 |
XM_047420768.1 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
NM_001378473.1 | chr7:g.140778038_140834818del56781 | c.139_1314del56781 | p.L47_P438del392 | RefSeq | GRCh38/hg38 |
XM_017012558 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
XM_047420767.1 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
NM_001354609.2 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
NM_001374244.1 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
XM_017012559 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
NM_001378472.1 | chr7:g.140778038_140834818del56781 | c.139_1314del56781 | p.L47_P438del392 | RefSeq | GRCh38/hg38 |
NM_004333.6 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
XM_047420766.1 | chr7:g.140781659_140834819del53161 | c.139_1314del53161 | p.L47_W438del392 | RefSeq | GRCh38/hg38 |
XM_017012559.2 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
NM_004333.5 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
NM_001374258.1 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
NM_001378474.1 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
NM_001378467.1 | chr7:g.140783031_140850213del67183 | c.139_1314del67183 | p.V47_R438del392 | RefSeq | GRCh38/hg38 |
NM_001378475.1 | chr7:g.140777028_140850212del73185 | c.139_1314del73185 | p.V47_A438del392 | RefSeq | GRCh38/hg38 |
NM_004333 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
XM_017012559.1 | chr7:g.140783142_140850213del67072 | c.139_1314del67072 | p.V47_L438del392 | RefSeq | GRCh38/hg38 |
NM_001378468.1 | chr7:g.140783022_140850213del67192 | c.141_1314+2del67192 | p.V47_M438del392 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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