ClinVar Miner

List of variants in gene SYN1 studied for X-linked epilepsy-learning disabilities-behavior disorders syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP
NC_000023.10:g.(?_47464357)_(47479147_?)dup
NM_006950.3(SYN1):c.1056-14_1056-8del rs377385507
NM_006950.3(SYN1):c.1063C>T (p.Leu355=) rs191822319
NM_006950.3(SYN1):c.1067G>A (p.Trp356Ter) rs137852560
NM_006950.3(SYN1):c.1107C>T (p.Ile369=) rs150248483
NM_006950.3(SYN1):c.1110C>T (p.Cys370=) rs141925310
NM_006950.3(SYN1):c.1137C>T (p.Asp379=) rs762471804
NM_006950.3(SYN1):c.1159-7C>T rs767722750
NM_006950.3(SYN1):c.1198G>A (p.Asp400Asn) rs772668988
NM_006950.3(SYN1):c.1297C>T (p.His433Tyr) rs41298474
NM_006950.3(SYN1):c.1310C>T (p.Pro437Leu) rs895517774
NM_006950.3(SYN1):c.1319G>A (p.Gly440Glu)
NM_006950.3(SYN1):c.1325T>C (p.Leu442Pro) rs375440874
NM_006950.3(SYN1):c.1363C>T (p.Pro455Ser) rs1371497364
NM_006950.3(SYN1):c.1369G>C (p.Ala457Pro) rs748323076
NM_006950.3(SYN1):c.1389A>C (p.Pro463=) rs1435656023
NM_006950.3(SYN1):c.1439dup (p.Leu481fs) rs1556857481
NM_006950.3(SYN1):c.1493C>T (p.Pro498Leu) rs1198466921
NM_006950.3(SYN1):c.150T>G (p.Thr50=) rs1556861816
NM_006950.3(SYN1):c.1516C>T (p.Gln506Ter)
NM_006950.3(SYN1):c.152C>G (p.Ala51Gly) rs187134574
NM_006950.3(SYN1):c.1615G>A (p.Gly539Ser) rs794727076
NM_006950.3(SYN1):c.1629T>C (p.Pro543=) rs1027134708
NM_006950.3(SYN1):c.1648G>A (p.Ala550Thr) rs397514680
NM_006950.3(SYN1):c.1663C>T (p.Gln555Ter) rs397514679
NM_006950.3(SYN1):c.1667G>T (p.Arg556Leu)
NM_006950.3(SYN1):c.1699A>G (p.Thr567Ala) rs200533370
NM_006950.3(SYN1):c.1701A>T (p.Thr567=) rs770195822
NM_006950.3(SYN1):c.1815C>T (p.Ser605=) rs1452773137
NM_006950.3(SYN1):c.1818G>A (p.Gln606=) rs967215240
NM_006950.3(SYN1):c.184T>G (p.Ser62Ala) rs1294224206
NM_006950.3(SYN1):c.189G>T (p.Pro63=) rs371739376
NM_006950.3(SYN1):c.1943C>T (p.Ala648Val) rs796053397
NM_006950.3(SYN1):c.1944C>T (p.Ala648=) rs1556857414
NM_006950.3(SYN1):c.1961G>A (p.Gly654Glu) rs749342768
NM_006950.3(SYN1):c.1968G>A (p.Pro656=) rs199844514
NM_006950.3(SYN1):c.213G>A (p.Ser71=)
NM_006950.3(SYN1):c.350T>C (p.Leu117Pro) rs1556861785
NM_006950.3(SYN1):c.360C>A (p.Asp120Glu) rs372165835
NM_006950.3(SYN1):c.371C>T (p.Thr124Ile) rs1339768860
NM_006950.3(SYN1):c.376T>A (p.Trp126Arg) rs1556861783
NM_006950.3(SYN1):c.426A>G (p.Lys142=) rs145911562
NM_006950.3(SYN1):c.473A>G (p.Asn158Ser) rs765486966
NM_006950.3(SYN1):c.506G>A (p.Arg169Gln) rs775109362
NM_006950.3(SYN1):c.526C>T (p.Arg176Trp) rs769458536
NM_006950.3(SYN1):c.528-2A>T rs1556860663
NM_006950.3(SYN1):c.579A>G (p.Ala193=) rs1556860653
NM_006950.3(SYN1):c.581G>A (p.Arg194His)
NM_006950.3(SYN1):c.756C>T (p.Tyr252=) rs1556860614
NM_006950.3(SYN1):c.838-8T>G rs12394306
NM_006950.3(SYN1):c.883G>A (p.Val295Met) rs1085307749
NM_006950.3(SYN1):c.912C>T (p.Ala304=) rs62636605
NM_006950.3(SYN1):c.939C>T (p.Asp313=) rs373928763
NM_006950.3(SYN1):c.944G>A (p.Arg315His)

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.