ClinVar Miner

List of variants reported as likely benign for Rolandic epilepsy with mental retardation and speech dyspraxia, X-linked

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_014467.3(SRPX2):c.1030C>A (p.Leu344Ile) rs149051060
NM_014467.3(SRPX2):c.1221A>G (p.Gln407=) rs375935170
NM_014467.3(SRPX2):c.1373G>A (p.Arg458Gln) rs146051561
NM_014467.3(SRPX2):c.224A>T (p.Lys75Met) rs767072861
NM_014467.3(SRPX2):c.257G>A (p.Arg86His) rs776691028
NM_014467.3(SRPX2):c.355+8G>T rs772952088
NM_014467.3(SRPX2):c.449C>T (p.Ser150Phe) rs373847965
NM_014467.3(SRPX2):c.693C>A (p.His231Gln) rs142719253
NM_014467.3(SRPX2):c.732T>C (p.Tyr244=) rs1556013511
NM_014467.3(SRPX2):c.809C>T (p.Pro270Leu) rs148735447
NM_014467.3(SRPX2):c.980A>G (p.Asn327Ser) rs121918363
NM_014467.3(SRPX2):c.982G>A (p.Val328Ile) rs753573260

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.