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Gene | PALB2 |
Variant | T226S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | PALB2 T226S lies within the DNA-binding and BRCA1-interacting regions of the Palb2 protein (UniProt.org). T226S has not been characterized in the scientific literature and therefore, its effect on Palb2 protein function is unknown (PubMed, Mar 2024). |
Associated Drug Resistance | |
Category Variants Paths |
PALB2 mutant PALB2 T226S |
Transcript | NM_024675.4 |
gDNA | chr16:g.23635869G>C |
cDNA | c.677C>G |
Protein | p.T226S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001407301.1 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407298.1 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_024675.3 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_024675.4 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407309.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407308.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407302.1 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
XM_017023673.2 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
XM_011545948.2 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407296.1 | chr16:g.23635809G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407304.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
XM_017023672.2 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
XM_017023672 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407306.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407299.1 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407310.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_024675 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407297.1 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407311.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
XM_017023673 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
XM_011545948 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407307.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407300.1 | chr16:g.23635869G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
NM_001407305.1 | chr16:g.23634984G>C | c.677C>G | p.T226S | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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