ClinVar Miner

List of variants in gene SPG7 reported as uncertain significance by GeneDx

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_003119.4(SPG7):c.1933T>A (p.Ser645Thr) rs2099104 0.00073
NM_003119.4(SPG7):c.2275G>A (p.Ala759Thr) rs140769107 0.00061
NM_003119.4(SPG7):c.1267G>A (p.Gly423Ser) rs201543030 0.00024
NM_003119.4(SPG7):c.220G>A (p.Gly74Arg) rs114854791 0.00022
NM_003119.4(SPG7):c.1939G>T (p.Ala647Ser) rs199689138 0.00017
NM_003119.4(SPG7):c.782C>T (p.Thr261Met) rs370949294 0.00014
NM_003119.4(SPG7):c.638G>A (p.Arg213Gln) rs147673636 0.00010
NM_003119.4(SPG7):c.584A>G (p.Tyr195Cys) rs145776296 0.00009
NM_003119.4(SPG7):c.1049C>A (p.Pro350His) rs376254211 0.00008
NM_003119.4(SPG7):c.1198C>T (p.Arg400Trp) rs748024868 0.00004
NM_003119.4(SPG7):c.1966C>T (p.Arg656Cys) rs536084933 0.00004
NM_003119.4(SPG7):c.566G>A (p.Ser189Asn) rs762049799 0.00004
NM_003119.4(SPG7):c.1305G>T (p.Gln435His) rs559906913 0.00003
NM_003119.4(SPG7):c.2191G>A (p.Ala731Thr) rs747521455 0.00003
NM_003119.4(SPG7):c.347C>T (p.Ser116Leu) rs149474131 0.00003
NM_003119.4(SPG7):c.445G>A (p.Ala149Thr) rs777638594 0.00003
NM_003119.4(SPG7):c.1771G>A (p.Val591Met) rs199804717 0.00002
NM_003119.4(SPG7):c.1795C>T (p.Arg599Trp) rs764645740 0.00002
NM_003119.4(SPG7):c.313A>T (p.Arg105Trp) rs374082677 0.00002
NM_003119.4(SPG7):c.359C>T (p.Ala120Val) rs530877336 0.00002
NM_003119.4(SPG7):c.388C>T (p.Arg130Cys) rs863224217 0.00002
NM_003119.4(SPG7):c.1054G>A (p.Gly352Ser) rs537421502 0.00001
NM_003119.4(SPG7):c.1115C>T (p.Ala372Val) rs776176403 0.00001
NM_003119.4(SPG7):c.1235C>T (p.Ala412Val) rs746668495 0.00001
NM_003119.4(SPG7):c.1573T>C (p.Cys525Arg) rs2058586638 0.00001
NM_003119.4(SPG7):c.1643C>A (p.Ala548Asp) rs863224220 0.00001
NM_003119.4(SPG7):c.1976A>G (p.Tyr659Cys) rs1052772091 0.00001
NM_003119.4(SPG7):c.2143G>A (p.Glu715Lys) rs374302115 0.00001
NM_003119.4(SPG7):c.2148G>C (p.Lys716Asn) rs776661222 0.00001
NM_003119.4(SPG7):c.2181G>A (p.Ala727=) rs753423781 0.00001
NM_003119.4(SPG7):c.2182C>G (p.Leu728Val) rs1433673841 0.00001
NM_003119.4(SPG7):c.2227A>C (p.Ile743Leu) rs372231786 0.00001
NM_003119.4(SPG7):c.2293G>A (p.Asp765Asn) rs374941242 0.00001
NM_003119.4(SPG7):c.2314G>T (p.Asp772Tyr) rs1235854891 0.00001
NM_003119.4(SPG7):c.416G>A (p.Arg139Gln) rs948625936 0.00001
NM_003119.4(SPG7):c.601G>A (p.Val201Met) rs775545751 0.00001
NM_003119.4(SPG7):c.703A>G (p.Ile235Val) rs191022979 0.00001
NM_003119.4(SPG7):c.898G>A (p.Gly300Arg) rs771060044 0.00001
NM_003119.4(SPG7):c.941T>C (p.Met314Thr) rs863224219 0.00001
GRCh37/hg19 16q24.3(chr16:89623304-89624182)x3
NM_003119.4(SPG7):c.1013G>A (p.Gly338Asp)
NM_003119.4(SPG7):c.1048C>A (p.Pro350Thr) rs199789849
NM_003119.4(SPG7):c.1166G>T (p.Arg389Leu)
NM_003119.4(SPG7):c.1171C>T (p.Arg391Trp) rs1057524520
NM_003119.4(SPG7):c.1193G>A (p.Arg398Gln) rs771782004
NM_003119.4(SPG7):c.1231G>A (p.Asp411Asn) rs745444834
NM_003119.4(SPG7):c.1261A>G (p.Met421Val)
NM_003119.4(SPG7):c.1324+4143C>T
NM_003119.4(SPG7):c.1364C>T (p.Thr455Met)
NM_003119.4(SPG7):c.1502C>T (p.Ser501Phe)
NM_003119.4(SPG7):c.1613C>G (p.Thr538Ser) rs1160298693
NM_003119.4(SPG7):c.1727C>G (p.Ser576Trp) rs151249432
NM_003119.4(SPG7):c.1760A>C (p.His587Pro) rs1057524632
NM_003119.4(SPG7):c.1904C>T (p.Ser635Leu) rs864622507
NM_003119.4(SPG7):c.2041G>C (p.Glu681Gln) rs863224221
NM_003119.4(SPG7):c.2047C>T (p.Leu683Phe) rs769512676
NM_003119.4(SPG7):c.2050A>T (p.Met684Leu)
NM_003119.4(SPG7):c.2098G>A (p.Asp700Asn) rs2058662790
NM_003119.4(SPG7):c.232TTG[2] (p.Leu80del) rs527363502
NM_003119.4(SPG7):c.412T>A (p.Tyr138Asn) rs863224218
NM_003119.4(SPG7):c.413A>C (p.Tyr138Ser) rs377268309
NM_003119.4(SPG7):c.498C>T (p.Ser166=) rs780508442
NM_003119.4(SPG7):c.544C>T (p.Arg182Cys)
NM_003119.4(SPG7):c.880C>G (p.Arg294Gly)

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