Variation name (cDNA level) | Variation name (protein level) | Variation status |
c.7553A>G | p.Asn2518Ser |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
AAT | Asn | AGT | Ser | A->G | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
Microtubule binding domain (ba | Yes, non coding strand | No |
At the mRNA level | On restriction map |
New restriction site(s): none Lost restriction site(s): none |
Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
---|---|---|
0.31 | 0.55 (non pathogenous) | 41 (Polymorphism) |
Sample ID | Patient status |
19_22079---22079-001 | Relative |
Symptom |
Reference ID | Reference |
19 | Unpublished data |