| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FANCA, LOC112486223 (L25R) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group A | |
| | FANCA, LOC112486223 (W22*) | Single nucleotide variant (nonsense) | not provided +2 more | GPathogenic/Likely pathogenic |
| | FANCA, LOC112486223 (R20K) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | FANCA, LOC112486223 (A10T) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group A +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi anemia complementation group A | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Fanconi anemia complementation group A | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group A | |
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