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| Gene | FANCA |
| Variant | L908P |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FANCA L908P does not lie within any known functional domains of the Fanca protein (UniProt.org). L908P has been identified in sequencing studies (PMID: 22895193), but has not been biochemically characterized and therefore, its effect on Fanca protein function is unknown (PubMed, Feb 2026). |
| Associated Drug Resistance | |
| Category Variants Paths |
FANCA mutant FANCA L908P |
| Transcript | NM_000135.4 |
| gDNA | chr16:g.89764945A>G |
| cDNA | c.2723T>C |
| Protein | p.L908P |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_011522946 | chr16:g.89742819A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_011522946.3 | chr16:g.89742819A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_017023044.2 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_005256294 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_011522945.2 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| NM_001286167.2 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_005256294.4 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| NM_001286167 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| NM_000135.4 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| NM_000135.3 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_017023045 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_017023045.1 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_011522945 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_011522947 | chr16:g.89742819A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| NM_001286167.3 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_024450189.1 | chr16:g.89742819A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| NM_000135 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_017023044 | chr16:g.89764945A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| XM_011522947.2 | chr16:g.89742819A>G | c.2723T>C | p.L908P | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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