ClinVar Miner

List of variants in gene SPG7 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_003119.4(SPG7):c.1552+244T>C rs462561 0.95430
NM_003119.4(SPG7):c.1324+4542A>G rs382745 0.46503
NM_003119.4(SPG7):c.1151-111A>G rs463701 0.45727
NM_003119.4(SPG7):c.618+12T>C rs3803679 0.45572
NM_003119.4(SPG7):c.1324+197C>T rs595869 0.44164
NM_003119.4(SPG7):c.286+46C>T rs3922633 0.43914
NM_003119.4(SPG7):c.184-132T>C rs3922634 0.43895
NM_003119.4(SPG7):c.1324+4020A>G rs647747 0.43709
NM_003119.4(SPG7):c.1324+308G>T rs680716 0.42590
NM_003119.4(SPG7):c.287-233G>A rs11076605 0.42573
NM_003119.4(SPG7):c.184-235G>A rs4238831 0.42308
NM_003119.4(SPG7):c.759-162G>A rs3803677 0.42305
NM_003119.4(SPG7):c.377-171G>A rs3803680 0.42187
NM_003119.4(SPG7):c.861+119C>T rs3803676 0.41924
NM_003119.4(SPG7):c.619-115C>T rs3935627 0.24728
NM_003119.4(SPG7):c.1552+205G>A rs2292952 0.21945
NM_003119.4(SPG7):c.1937-54A>G rs730264 0.20039
NM_003119.4(SPG7):c.1450-29G>A rs462464 0.20021
NM_003119.4(SPG7):c.1552+65A>C rs461405 0.19628
NM_003119.4(SPG7):c.1779+47G>C rs3794632 0.19456
NM_003119.4(SPG7):c.1664-344T>C rs7359417 0.17643
NM_003119.4(SPG7):c.1664-130G>T rs71396924 0.17533
NM_003119.4(SPG7):c.1664-177C>T rs71396923 0.17081
NM_003119.4(SPG7):c.1664-112G>A rs66845605 0.17001
NM_003119.4(SPG7):c.287-280A>G rs35463145 0.14451
NM_003119.4(SPG7):c.758+322C>T rs34607811 0.13953
NM_003119.4(SPG7):c.1324+3841dup rs149246489 0.12932
NM_003119.4(SPG7):c.1507A>G (p.Thr503Ala) rs2292954 0.12849
NM_003119.4(SPG7):c.2063G>A (p.Arg688Gln) rs12960 0.12801
NM_003119.4(SPG7):c.1324+3850T>C rs182897688 0.11337
NM_003119.4(SPG7):c.1449+19G>A rs79201073 0.07399
NM_003119.4(SPG7):c.*33C>T rs60711430 0.03853
NM_003119.4(SPG7):c.1936+154G>T rs8044175 0.03831
NM_003119.4(SPG7):c.2292C>T (p.Ile764=) rs61747711 0.02864
NM_003119.4(SPG7):c.619-50C>T rs74037215 0.02679
NM_003119.4(SPG7):c.987+290C>A rs74037218 0.02597
NM_003119.4(SPG7):c.1324+3941G>C rs150127651 0.02273
NM_003119.4(SPG7):c.1552+231C>T rs78210031 0.01838
NM_003119.4(SPG7):c.1770C>T (p.Ala590=) rs60488729 0.01823
NM_003119.4(SPG7):c.2037G>A (p.Ala679=) rs79756036 0.01778
NM_003119.4(SPG7):c.1779+238A>G rs17177403 0.01518
NM_003119.4(SPG7):c.2188A>G (p.Asn730Asp) rs35749032 0.01431
NM_003119.4(SPG7):c.881G>A (p.Arg294His) rs115661328 0.01169
NM_003119.4(SPG7):c.2295C>T (p.Asp765=) rs61747712 0.01110
NM_003119.4(SPG7):c.1653C>T (p.Arg551=) rs56031686 0.00386
NM_003119.4(SPG7):c.1324+10C>T rs202070075 0.00073
NM_003119.4(SPG7):c.1324+148dup rs11403793
NM_003119.4(SPG7):c.1324+3816GGTGAGGCG[2] rs543538383
NM_003119.4(SPG7):c.1324+3849_1324+3850insCGGGCGAGGCGGGCGAGG rs1567918794
NM_003119.4(SPG7):c.1324+3852A>G rs1238669262
NM_003119.4(SPG7):c.1324+3893_1324+3894insAGGTGAGGTGAGGC rs1555613855
NM_003119.4(SPG7):c.1324+4109C>A rs199969908
NM_003119.4(SPG7):c.1324+4109C>T rs199969908
NM_003119.4(SPG7):c.1449+174C>T rs78718968
NM_003119.4(SPG7):c.1450-75del rs35936864
NM_003119.4(SPG7):c.1450-75dup rs35936864
NM_003119.4(SPG7):c.1450-78C>T rs577802159
NM_003119.4(SPG7):c.184-4del rs5818722
NM_003119.4(SPG7):c.377-245_377-244insTCTCA rs59761318
NM_003119.4(SPG7):c.618+170C>T rs8051680
NM_003119.4(SPG7):c.619-47G>A rs3935626
NM_003119.4(SPG7):c.759-126C>T rs74037217
NM_003119.4(SPG7):c.862-34G>T rs4785690
NM_003119.4(SPG7):c.987+5A>G rs4785691

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