ClinVar Miner

List of variants in gene STXBP2 reported as likely pathogenic

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_006949.4(STXBP2):c.389T>C (p.Leu130Ser) rs930347206 0.00009
NM_006949.4(STXBP2):c.1001C>T (p.Pro334Leu) rs747031778 0.00004
NM_006949.4(STXBP2):c.194G>A (p.Arg65Gln) rs141717050 0.00004
NM_006949.4(STXBP2):c.1214G>A (p.Arg405Gln) rs773360200 0.00002
NM_006949.4(STXBP2):c.704G>A (p.Arg235Gln) rs757488006 0.00001
NC_000019.9:g.(?_7703306)_(7707110_?)del
NC_000019.9:g.(?_7706571)_(7712696_?)del
NM_006949.4(STXBP2):c.1026+1G>T
NM_006949.4(STXBP2):c.1026+2T>A
NM_006949.4(STXBP2):c.1044_1051del (p.His348fs)
NM_006949.4(STXBP2):c.1107+1G>C
NM_006949.4(STXBP2):c.1107+2T>G
NM_006949.4(STXBP2):c.1108-1G>A
NM_006949.4(STXBP2):c.1115C>A (p.Ala372Asp) rs1434458616
NM_006949.4(STXBP2):c.1138G>T (p.Glu380Ter)
NM_006949.4(STXBP2):c.1179del (p.Leu394fs)
NM_006949.4(STXBP2):c.1210dup (p.Ile404fs)
NM_006949.4(STXBP2):c.1279C>T (p.Gln427Ter)
NM_006949.4(STXBP2):c.1356+1G>C
NM_006949.4(STXBP2):c.1356+1G>T
NM_006949.4(STXBP2):c.1411C>T (p.Gln471Ter)
NM_006949.4(STXBP2):c.143C>G (p.Ser48Ter)
NM_006949.4(STXBP2):c.1452+1G>A
NM_006949.4(STXBP2):c.1525C>T (p.Gln509Ter) rs760061071
NM_006949.4(STXBP2):c.1538+1G>C
NM_006949.4(STXBP2):c.1539-2A>G
NM_006949.4(STXBP2):c.1610_1611dup (p.Val538fs)
NM_006949.4(STXBP2):c.1611T>G (p.Tyr537Ter)
NM_006949.4(STXBP2):c.1621G>A (p.Gly541Ser) rs61736587
NM_006949.4(STXBP2):c.169+2T>G rs1555768979
NM_006949.4(STXBP2):c.1697G>A (p.Gly566Asp)
NM_006949.4(STXBP2):c.246+1G>T
NM_006949.4(STXBP2):c.247-1G>T
NM_006949.4(STXBP2):c.247-2A>C rs921624651
NM_006949.4(STXBP2):c.247-2A>G
NM_006949.4(STXBP2):c.247-2_284del
NM_006949.4(STXBP2):c.255_265del (p.Ala86fs)
NM_006949.4(STXBP2):c.290dup (p.Thr98fs)
NM_006949.4(STXBP2):c.326-1G>C rs2031844309
NM_006949.4(STXBP2):c.37+596_82delinsCAGCTCTGAGGCATGCCTAGCTGAGGCTATCCCACTGACCTCCGGTCTCAGTTTCCTCATCTGTAAAATGGAATCACTTTTTTCTAATCTCCCCCAATTAAAGGGGTTTGAGCTACAGACCGCCCTGCCTAGAGGAGAGAGTGGAGAGAAGTAACGGGGTGGCCCCGCCCAGCCACGTCCACTGTGTCATGTCCACTGTTATCAAGACGGCCAG
NM_006949.4(STXBP2):c.37+5G>A
NM_006949.4(STXBP2):c.429+1G>A
NM_006949.4(STXBP2):c.429+1G>C
NM_006949.4(STXBP2):c.474_483delinsGA (p.Cys158fs) rs1599397070
NM_006949.4(STXBP2):c.652dup (p.Ser218fs)
NM_006949.4(STXBP2):c.703C>G (p.Arg235Gly) rs753879238
NM_006949.4(STXBP2):c.80del (p.Glu27fs)
NM_006949.4(STXBP2):c.87+1G>A
NM_006949.4(STXBP2):c.87+2T>C
NM_006949.4(STXBP2):c.902+1G>A
NM_006949.4(STXBP2):c.960+1G>T

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