By variant position
By protein location
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By mutation
By inheritance
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Latest mutation
Table legend
| Number | Exon/Intron | Nucleotide change | Protein change | Location | Mutation type | Consequences | Phenotype | Inheritance | Reference |
|---|---|---|---|---|---|---|---|---|---|
| 309 | 7 | c.980T>G | p.Leu327Arg | DIS5-S6 | Missense | N→P/﹢ (102) | SMEI | Both mosaic | de Lange IM.2018 |
Inheritance information:
| Number | Nucleotide change | Protein change | Mutation type | Proband's phenotype | 1st transmitter's phenotype | Mosaic | Affected generations | Penetrance | Reference |
|---|---|---|---|---|---|---|---|---|---|
| 36 | c.980T>G | p.Leu327Arg(DIS5-S6) | Missense | SMEI | NA | both mosaic (34% and 12%) | de Lange IM.2018 |
Copyright ©2014 Institute of Neuroscience and The Second Affiliated Hospital of Guangzhou Medical University
Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China
Collaborative Innovation Center for Neurogenetics and Channelopathies, Guangzhou 510260, China.