Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.IVS30+28C>A (c.3838+28C>A) | Heterozygous | Polymorphism? |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
GAT | Asp | spl+28 | Spl. | C->A | Tv |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
cb EGF-like #17 | Ca2+ binding |
At the mRNA level | On restriction map |
Not tested on cDNA (needed) | New restriction site(s): none Lost restriction site(s): none |
Impact on splicing | ||||||||||
Splice site type | Wild type sequence | CV | Mutant type sequence | CV | Variation (%) | |||||
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
USA08PIT F0011 I01 | Proband | NA | NA | ? | U.S.A |
Phenotypic group | Disease |
NA | Classical MFS |
Symptom |
no clinical data |
Reference ID | PubMed ID | Reference |
49 | 10533071 | Yuan B, Thomas JP, von Kodolitsch Y, Pyeritz RE. "Comparison of heteroduplex analysis, direct sequencing, and enzyme mismatch cleavage for detecting mutations in a large gene, FBN1". Hum Mutat 1999;14(5):440-6 . |