ClinVar Miner

List of variants reported as benign for Brugada syndrome

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Total variants: 33
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HGVS dbSNP
NM_000719.7(CACNA1C):c.*1109dup rs11429670
NM_000719.7(CACNA1C):c.*284C>T rs11062319
NM_000719.7(CACNA1C):c.*3903del rs11353034
NM_000719.7(CACNA1C):c.*4090G>A rs7316246
NM_000719.7(CACNA1C):c.*4273A>G rs7302540
NM_000719.7(CACNA1C):c.*4299C>A rs12809807
NM_000719.7(CACNA1C):c.*4611T>G rs10466907
NM_000719.7(CACNA1C):c.*4831T>A rs4765975
NM_000719.7(CACNA1C):c.*5267C>A rs7957163
NM_000719.7(CACNA1C):c.*5421del rs10713809
NM_000719.7(CACNA1C):c.*5970A>C rs4765976
NM_000719.7(CACNA1C):c.*659_*660insGAAGGGGCCGCCGG rs71057834
NM_000719.7(CACNA1C):c.2436C>T (p.Asp812=) rs215976
NM_000719.7(CACNA1C):c.3786C>T (p.Phe1262=) rs216008
NM_000719.7(CACNA1C):c.4485T>C (p.Asp1495=) rs41276710
NM_000719.7(CACNA1C):c.522G>A (p.Ala174=) rs1544514
NM_000719.7(CACNA1C):c.5360C>T (p.Thr1787Met) rs192749597
NM_000719.7(CACNA1C):c.5361G>A (p.Thr1787=) rs1051375
NM_000722.4(CACNA2D1):c.355-5del rs142849270
NM_001037.5(SCN1B):c.40+15G>T rs72556351
NM_001267550.2(TTN):c.17048A>G (p.Tyr5683Cys) rs72648942
NM_006514.3(SCN10A):c.1157T>G (p.Phe386Cys) rs78555408
NM_006514.3(SCN10A):c.3133C>A (p.Pro1045Thr) rs73062575
NM_006514.3(SCN10A):c.4710G>A (p.Thr1570=) rs78425180
NM_006514.3(SCN10A):c.5089G>A (p.Val1697Ile) rs77804526
NM_006514.3(SCN10A):c.5217C>T (p.Asp1739=) rs116353929
NM_006514.3(SCN10A):c.618A>G (p.Ile206Met) rs74717885
NM_007159.4(SLMAP):c.1866T>A (p.Leu622=) rs35219531
NM_007159.4(SLMAP):c.2043G>A (p.Gln681=) rs17745496
NM_007159.4(SLMAP):c.828+11C>A rs2306056
NM_198056.2(SCN5A):c.1441C>T (p.Arg481Trp) rs144511230
NM_198056.2(SCN5A):c.274-25_274-24delinsAT rs386660280
NM_198056.2(SCN5A):c.3578G>A (p.Arg1193Gln) rs41261344

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