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Gene | PALB2 |
Variant | V932M |
Impact List | missense |
Protein Effect | no effect |
Gene Variant Descriptions | PALB2 V932M lies within WD repeat 2 of the Palb2 protein (UniProt.org). V932M results in Brca2 binding, Rad51 foci formation, and recruitment to DNA damage sites similar to wild-type Palb2 in cultured cells (PMID: 31586400), and does not demonstrate reduced homology-directed DNA repair activity compared to wild-type in cultured cells (PMID: 31586400, PMID: 31636395, PMID: 33964450). |
Associated Drug Resistance | |
Category Variants Paths |
PALB2 mutant PALB2 V932M |
Transcript | NM_024675.4 |
gDNA | chr16:g.23624049C>T |
cDNA | c.2794G>A |
Protein | p.V932M |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_024675.3 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
NM_001407299.1 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
XM_017023672.2 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
NM_001407301.1 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
NM_001407300.1 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
NM_024675.4 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
NM_024675 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
XM_017023673.2 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
XM_017023672 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
XM_017023673 | chr16:g.23624049C>T | c.2794G>A | p.V932M | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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