ClinVar Miner

List of variants in gene SEC63 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_007214.5(SEC63):c.1936-132T>C rs570558 0.97813
NM_007214.5(SEC63):c.2035-125A>G rs579120 0.97809
NM_007214.5(SEC63):c.340-175_340-174dup rs4029185 0.97809
NM_007214.5(SEC63):c.-77C>T rs2272884 0.94610
NM_007214.5(SEC63):c.*123T>A rs503068 0.88225
NM_007214.5(SEC63):c.2139+287A>G rs494630 0.87244
NM_007214.5(SEC63):c.564C>T (p.Asn188=) rs675117 0.87051
NM_007214.5(SEC63):c.625-107T>A rs617920 0.87028
NM_007214.5(SEC63):c.1833+252G>T rs12193403 0.81676
NM_007214.5(SEC63):c.1055-220T>G rs2272886 0.76693
NM_007214.5(SEC63):c.1441-260T>C rs11153090 0.71405
NM_007214.5(SEC63):c.961+129A>C rs6906940 0.19612
NM_007214.5(SEC63):c.452+322T>C rs9400161 0.10648
NM_007214.5(SEC63):c.1358-128A>G rs9373986 0.10568
NM_007214.5(SEC63):c.1936-186A>G rs17068939 0.05136
NM_007214.5(SEC63):c.624+308C>T rs6938094 0.05114
NM_007214.5(SEC63):c.574-59A>T rs6922398 0.05112
NM_007214.5(SEC63):c.224+105A>G rs2818197 0.04771
NM_007214.5(SEC63):c.225-162C>T rs6905131 0.04169
NM_007214.5(SEC63):c.1666G>A (p.Val556Ile) rs17854547 0.03299
NM_007214.5(SEC63):c.124+94C>T rs58259286 0.02446
NM_007214.5(SEC63):c.2027C>T (p.Thr676Ile) rs61733388 0.01749
NM_007214.5(SEC63):c.340-12del rs58827902 0.01010
NM_007214.5(SEC63):c.340-12G>T rs2064201 0.00438
NM_007214.5(SEC63):c.363A>G (p.Lys121=) rs146677514 0.00308
NM_007214.5(SEC63):c.2134T>C (p.Leu712=) rs61733387 0.00201
NM_007214.5(SEC63):c.515-18A>G rs370955001 0.00103
NM_007214.5(SEC63):c.1278C>T (p.Phe426=) rs146559698 0.00093
NM_007214.5(SEC63):c.340-7T>C rs1569557 0.00081
NM_007214.5(SEC63):c.1441-4C>G rs200112157 0.00071
NM_007214.5(SEC63):c.1674T>C (p.Asn558=) rs143570743 0.00060
NM_007214.5(SEC63):c.807G>A (p.Thr269=) rs182467867 0.00009
NM_007214.5(SEC63):c.515-7A>G rs377577480 0.00008
NM_007214.5(SEC63):c.2205G>C (p.Gly735=) rs761321161 0.00003
NM_007214.5(SEC63):c.108C>T (p.Pro36=) rs202122513 0.00001
NC_000006.12:g.107958342T>G rs6903090
NM_007214.5(SEC63):c.1210-18dup rs370485907
NM_007214.5(SEC63):c.1210-7del rs370485907
NM_007214.5(SEC63):c.124+20G>A rs114539321
NM_007214.5(SEC63):c.1323T>C (p.Ser441=)
NM_007214.5(SEC63):c.1358-16dup
NM_007214.5(SEC63):c.1371A>G (p.Glu457=)
NM_007214.5(SEC63):c.1674+17C>T
NM_007214.5(SEC63):c.1675-3del
NM_007214.5(SEC63):c.1697AAG[2] (p.Glu568del) rs752018806
NM_007214.5(SEC63):c.1834-10dup
NM_007214.5(SEC63):c.1881A>G (p.Leu627=)
NM_007214.5(SEC63):c.1936-11_1936-9del rs749125299
NM_007214.5(SEC63):c.1936-27_1936-25dup rs749125299
NM_007214.5(SEC63):c.1936-27_1936-26dup rs749125299
NM_007214.5(SEC63):c.2139+294dup rs35422686
NM_007214.5(SEC63):c.2140-97G>A rs642954
NM_007214.5(SEC63):c.339+149_339+151del rs71740089
NM_007214.5(SEC63):c.340-12_340-10del rs200904488
NM_007214.5(SEC63):c.340-12_340-11del rs139413431
NM_007214.5(SEC63):c.340-12_340-7del rs398124248
NM_007214.5(SEC63):c.340-12_340-8del rs747514864
NM_007214.5(SEC63):c.340-12_340-9del rs201981258
NM_007214.5(SEC63):c.340-13_340-12insCCC rs1554237230
NM_007214.5(SEC63):c.340-144T>G rs1008481
NM_007214.5(SEC63):c.340-6_340-4dup rs142388422
NM_007214.5(SEC63):c.625-10dup
NM_007214.5(SEC63):c.734-6del
NM_007214.5(SEC63):c.829-18T>C
NM_007214.5(SEC63):c.961+14C>T rs143606782

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