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| Gene | FANCA |
| Variant | S46P |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FANCA S46P does not lie within any known functional domains of the Fanca protein (UniProt.org). S46P has not been characterized in the scientific literature and therefore, its effect on Fanca protein function is unknown (PubMed, Nov 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
FANCA mutant FANCA S46P |
| Transcript | NM_000135.4 |
| gDNA | chr16:g.89815930A>G |
| cDNA | c.136T>C |
| Protein | p.S46P |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_017023046 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_005256294.4 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001286167.3 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_011522948 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001351830.1 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_017023044 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001286167.2 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_011522945.2 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001286167 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001351830.2 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001018112.3 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_011522948.2 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_000135 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001018112.2 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_017023045 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_017023046.1 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_001018112 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_011522945 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_000135.4 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_005256294 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| NM_000135.3 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_017023045.1 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| XM_017023044.2 | chr16:g.89815930A>G | c.136T>C | p.S46P | RefSeq | GRCh38/hg38 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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