ClinVar Miner

List of variants in gene DSP reported by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 38
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HGVS dbSNP
NM_004415.4(DSP):c.1034A>G (p.Asp345Gly) rs753855393
NM_004415.4(DSP):c.1090A>G (p.Ile364Val) rs886038909
NM_004415.4(DSP):c.1140+6T>C rs534740669
NM_004415.4(DSP):c.1562A>C (p.Asp521Ala) rs748790273
NM_004415.4(DSP):c.1790C>T (p.Ser597Leu) rs606231294
NM_004415.4(DSP):c.2071C>T (p.Leu691Phe) rs1363445022
NM_004415.4(DSP):c.269A>G (p.Gln90Arg) rs188516326
NM_004415.4(DSP):c.2933T>A (p.Ile978Lys) rs1060500615
NM_004415.4(DSP):c.3200C>T (p.Ala1067Val) rs1317030435
NM_004415.4(DSP):c.3338G>A (p.Arg1113Gln) rs768455823
NM_004415.4(DSP):c.3701A>G (p.Asn1234Ser) rs185367490
NM_004415.4(DSP):c.3706A>G (p.Arg1236Gly) rs377098318
NM_004415.4(DSP):c.3862A>C (p.Lys1288Gln) rs138907450
NM_004415.4(DSP):c.3877A>G (p.Ile1293Val) rs376555665
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly) rs28763965
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu) rs186842903
NM_004415.4(DSP):c.478C>T (p.Arg160Ter) rs397516943
NM_004415.4(DSP):c.4822C>T (p.Gln1608Ter) rs1060500610
NM_004415.4(DSP):c.4901G>A (p.Arg1634Gln) rs144106775
NM_004415.4(DSP):c.5035C>T (p.His1679Tyr) rs762561997
NM_004415.4(DSP):c.5353G>A (p.Glu1785Lys) rs528041468
NM_004415.4(DSP):c.5460dup (p.Val1821fs) rs1554108609
NM_004415.4(DSP):c.5498A>T (p.Glu1833Val) rs78652302
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn) rs41302885
NM_004415.4(DSP):c.6248G>A (p.Arg2083His) rs574637009
NM_004415.4(DSP):c.6269A>G (p.Glu2090Gly) rs755069593
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly) rs147000526
NM_004415.4(DSP):c.6902T>C (p.Ile2301Thr) rs772381363
NM_004415.4(DSP):c.7487_7488TG[2] (p.Cys2497_Glu2498delinsTer) rs754354190
NM_004415.4(DSP):c.7885G>A (p.Glu2629Lys) rs756976948
NM_004415.4(DSP):c.7915C>T (p.Arg2639Trp) rs771553674
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln) rs116888866
NM_004415.4(DSP):c.8529_8540del (p.2827_2830SGSR[4]) rs794728151
NM_004415.4(DSP):c.889G>A (p.Asp297Asn) rs201930322
NM_004415.4(DSP):c.88G>A (p.Val30Met) rs121912998
NM_004415.4(DSP):c.935_937del (p.Phe312del) rs794728138
NM_004415.4(DSP):c.939+1G>A rs727504443
NM_004415.4(DSP):c.943C>T (p.Arg315Cys) rs200476515

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