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| Gene | FANCA |
| Variant | H1355L |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FANCA H1355L does not lie within any known functional domains of the Fanca protein (UniProt.org). H1355L has been identified in sequencing studies (PMID: 32546565), 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 H1355L |
| Transcript | NM_000135.4 |
| gDNA | chr16:g.89739236T>A |
| cDNA | c.4064A>T |
| Protein | p.H1355L |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001286167 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| XM_005256294 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| NM_000135 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| NM_001286167.3 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| NM_001286167.2 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| NM_000135.4 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| NM_000135.3 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| XM_005256294.4 | chr16:g.89739236T>A | c.4064A>T | p.H1355L | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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