| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.842G>A | p.Gly281Glu | Heterozygous | LIKELY CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGG | Gly | GAG | Glu | G->A | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Pem,NM,NMH,FA,HD | Yes, non coding strand | No |
| Other variation(s) reported for this sample: c.IVS3-6C>A (c.655-6C>A) |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): Bsu36 I |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0 | - | 94 (Pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 02-GE18-G12A- | Proband | Female | 17 |
| Phenotypic group | Disease |
| Please contact curator |
| Reference ID | PubMed ID | Reference |
| 13 | 16563611 | J*ger, A. C., Friis-Hansen, L., Hansen, T. V. O., Eskildsen, P. C., S¿lling, K., Knigge, U., ? Nielsen, F. C. (2006). Characteristics of the Danish families with multiple endocrine neoplasia type 1. Molecular and Cellular Endocrinology, 249(1-2), 123?32. doi:10.1016/j.mce.2006.02.008 |