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| Gene | FANCA |
| Variant | Q1307Sfs*6 |
| Impact List | frameshift |
| Protein Effect | unknown |
| Gene Variant Descriptions | FANCA Q1307Sfs*6 indicates a shift in the reading frame starting at amino acid 1307 and terminating 6 residues downstream causing a premature truncation of the 1455 amino acid Fanca protein (UniProt.org). Q1307Sfs*6 has been identified in the scientific literature (PMID: 36181052), 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 Q1307Sfs*6 |
| Transcript | NM_000135.4 |
| gDNA | chr16:g.89740012dupA |
| cDNA | c.3918dupT |
| Protein | p.Q1307Sfs*6 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000135.4 | chr16:g.89740012dupA | c.3918dupT | p.Q1307Sfs*6 | RefSeq | GRCh38/hg38 |
| NM_001286167.3 | chr16:g.89740012dupA | c.3918dupT | p.Q1307Sfs*6 | RefSeq | GRCh38/hg38 |
| XM_005256294.4 | chr16:g.89740012dupA | c.3918dupT | p.Q1307Sfs*6 | RefSeq | GRCh38/hg38 |
| NM_001286167.2 | chr16:g.89740012dupA | c.3918dupT | p.Q1307Sfs*6 | RefSeq | GRCh38/hg38 |
| NM_000135.3 | chr16:g.89740012dupA | c.3918dupT | p.Q1307Sfs*6 | RefSeq | GRCh38/hg38 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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