ClinVar Miner

List of variants in gene SYN1 reported as likely benign for X-linked epilepsy-learning disabilities-behavior disorders syndrome

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_006950.3(SYN1):c.1063C>T (p.Leu355=) rs191822319
NM_006950.3(SYN1):c.1137C>T (p.Asp379=) rs762471804
NM_006950.3(SYN1):c.1159-7C>T rs767722750
NM_006950.3(SYN1):c.1389A>C (p.Pro463=) rs1435656023
NM_006950.3(SYN1):c.150T>G (p.Thr50=) rs1556861816
NM_006950.3(SYN1):c.1629T>C (p.Pro543=) rs1027134708
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.189G>T (p.Pro63=) rs371739376
NM_006950.3(SYN1):c.1944C>T (p.Ala648=) rs1556857414
NM_006950.3(SYN1):c.1968G>A (p.Pro656=) rs199844514
NM_006950.3(SYN1):c.579A>G (p.Ala193=) rs1556860653
NM_006950.3(SYN1):c.756C>T (p.Tyr252=) rs1556860614
NM_006950.3(SYN1):c.939C>T (p.Asp313=) rs373928763

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