ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely pathogenic

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Total variants: 25
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HGVS dbSNP
NC_000002.11:g.(?_167055131)_(167168316_?)dup
NM_001365536.1(SCN9A):c.1198G>A (p.Val400Met) rs1553491169
NM_001365536.1(SCN9A):c.1314+1G>T rs1295192882
NM_001365536.1(SCN9A):c.2517+1G>C
NM_001365536.1(SCN9A):c.2517G>T (p.Leu839=)
NM_001365536.1(SCN9A):c.2576T>C (p.Ile859Thr) rs80356474
NM_001365536.1(SCN9A):c.2600G>A (p.Gly867Asp) rs879254102
NM_001365536.1(SCN9A):c.2719C>T (p.Arg907Trp) rs202152511
NM_001365536.1(SCN9A):c.2720G>A (p.Arg907Gln)
NM_001365536.1(SCN9A):c.3019C>T (p.Arg1007Cys) rs121908910
NM_001365536.1(SCN9A):c.3204del (p.Lys1068fs) rs1574843584
NM_001365536.1(SCN9A):c.3925-2A>G
NM_001365536.1(SCN9A):c.4398+2T>C
NM_001365536.1(SCN9A):c.4399-1C>T rs1283839545
NM_001365536.1(SCN9A):c.4424_4427del (p.Thr1475fs) rs1574706911
NM_001365536.1(SCN9A):c.4503+1G>A rs746241591
NM_001365536.1(SCN9A):c.4503+1G>T rs746241591
NM_001365536.1(SCN9A):c.4507A>T (p.Lys1503Ter) rs876661206
NM_001365536.1(SCN9A):c.4733G>A (p.Trp1578Ter) rs200070962
NM_001365536.1(SCN9A):c.4868T>C (p.Leu1623Pro) rs1131691776
NM_001365536.1(SCN9A):c.5392G>T (p.Glu1798Ter) rs770416478
NM_001365536.1(SCN9A):c.5569del (p.Asp1857fs) rs1553472910
NM_001365536.1(SCN9A):c.5876A>C (p.Asp1959Ala) rs1060502047
NM_001365536.1(SCN9A):c.902-2A>C rs773824421
NM_001365536.1(SCN9A):c.965+1G>T

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