ClinVar Miner

List of variants in gene ADAMTS13 reported as not provided

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_139027.6(ADAMTS13):c.3178C>T (p.Arg1060Trp) rs142572218 0.00088
NM_139027.6(ADAMTS13):c.3773C>T (p.Ser1258Leu) rs142060916 0.00016
NM_139027.6(ADAMTS13):c.1816G>C (p.Ala606Pro) rs281875290 0.00006
NM_139027.6(ADAMTS13):c.3487C>T (p.Arg1163Trp) rs281875339 0.00003
NM_139027.6(ADAMTS13):c.911A>G (p.Tyr304Cys) rs281875285 0.00003
NM_139027.6(ADAMTS13):c.1520G>A (p.Arg507Gln) rs281875296 0.00002
NM_139027.6(ADAMTS13):c.1058C>T (p.Pro353Leu) rs281875338 0.00001
NM_139027.6(ADAMTS13):c.1170G>C (p.Trp390Cys) rs281875306 0.00001
NM_139027.6(ADAMTS13):c.1787C>T (p.Ala596Val) rs281875299 0.00001
NM_139027.6(ADAMTS13):c.1973A>G (p.Tyr658Cys) rs281875335 0.00001
NM_139027.6(ADAMTS13):c.3367C>T (p.Arg1123Cys) rs281875340 0.00001
NM_139027.6(ADAMTS13):c.3838C>T (p.Arg1280Trp) rs281875308 0.00001
NM_139027.6(ADAMTS13):c.577C>T (p.Arg193Trp) rs281875287 0.00001
NM_139027.6(ADAMTS13):c.1039T>A (p.Cys347Ser) rs281875294
NM_139027.6(ADAMTS13):c.1045C>T (p.Arg349Cys) rs281875288
NM_139027.6(ADAMTS13):c.1523G>A (p.Cys508Tyr) rs281875305
NM_139027.6(ADAMTS13):c.1574G>A (p.Gly525Asp) rs281875286
NM_139027.6(ADAMTS13):c.2012C>T (p.Pro671Leu) rs281875295
NM_139027.6(ADAMTS13):c.2017A>T (p.Ile673Phe) rs281875307
NM_139027.6(ADAMTS13):c.2272T>C (p.Cys758Arg) rs281875300
NM_139027.6(ADAMTS13):c.237C>G (p.Ile79Met) rs281875297
NM_139027.6(ADAMTS13):c.262G>A (p.Val88Met) rs281875302
NM_139027.6(ADAMTS13):c.2723G>A (p.Cys908Tyr) rs281875301
NM_139027.6(ADAMTS13):c.2723G>C (p.Cys908Ser) rs281875301
NM_139027.6(ADAMTS13):c.3401-3C>A
NM_139027.6(ADAMTS13):c.3548G>T (p.Gly1183Val) rs281875303
NM_139027.6(ADAMTS13):c.356C>T (p.Ser119Phe) rs281875291
NM_139027.6(ADAMTS13):c.533T>C (p.Ile178Thr) rs281875289
NM_139027.6(ADAMTS13):c.607T>C (p.Ser203Pro) rs281875298
NM_139027.6(ADAMTS13):c.695T>A (p.Leu232Gln) rs281875292
NM_139027.6(ADAMTS13):c.702C>A (p.His234Gln) rs281875304
NM_139027.6(ADAMTS13):c.703G>C (p.Asp235His) rs281875337
NM_139027.6(ADAMTS13):c.932G>A (p.Cys311Tyr) rs281875336

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