ClinVar Miner

List of variants in gene SUFU reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_016169.4(SUFU):c.*1122C>T rs11596235 0.23724
NM_016169.4(SUFU):c.*2585T>C rs11191355 0.20858
NM_016169.4(SUFU):c.*2668C>T rs11594179 0.17207
NM_016169.4(SUFU):c.*1373C>T rs17114808 0.14776
NM_016169.4(SUFU):c.*391A>G rs2298278 0.14670
NM_016169.4(SUFU):c.1299T>C (p.Ile433=) rs17114803 0.14628
NM_016169.4(SUFU):c.*1715A>G rs11818043 0.14606
NM_016169.4(SUFU):c.*1633C>T rs17114810 0.14323
NM_016169.4(SUFU):c.*1675G>A rs41287466 0.03346
NM_016169.4(SUFU):c.*3086A>G rs73342651 0.01014
NM_016169.4(SUFU):c.*1672A>G rs117196884 0.01007
NM_016169.4(SUFU):c.*205G>A rs115428806 0.00961
NM_016169.4(SUFU):c.*118C>T rs2298277 0.00835
NM_016169.4(SUFU):c.1018G>T (p.Ala340Ser) rs34135067 0.00646
NM_016169.4(SUFU):c.*3290C>G rs112808377 0.00612
NM_016169.4(SUFU):c.1291T>C (p.Leu431=) rs141950577 0.00487
NM_016169.4(SUFU):c.*2157C>T rs181690906 0.00474
NM_016169.4(SUFU):c.210T>C (p.Tyr70=) rs35166585 0.00430
NM_016169.4(SUFU):c.*2720C>T rs41287468 0.00417
NM_016169.4(SUFU):c.*505T>G rs116570216 0.00412
NM_016169.4(SUFU):c.*2172G>A rs540579682 0.00367
NM_016169.4(SUFU):c.*3268G>C rs150653416 0.00308
NM_016169.4(SUFU):c.*61G>A rs184505927 0.00249
NM_016169.4(SUFU):c.528C>T (p.His176=) rs150569584 0.00148
NM_016169.4(SUFU):c.910+14C>T rs202247757 0.00139
NM_016169.4(SUFU):c.600C>T (p.Ile200=) rs149513330 0.00116
NM_016169.4(SUFU):c.*476A>G rs575192580 0.00066
NM_016169.4(SUFU):c.*2729T>C rs574630127 0.00045
NM_016169.4(SUFU):c.*2956C>T rs562546771 0.00033
NM_016169.4(SUFU):c.*1936C>T rs118033896 0.00027
NM_016169.4(SUFU):c.*1997A>G rs757368847 0.00021
NM_016169.4(SUFU):c.1445C>T (p.Pro482Leu) rs765358771 0.00020
NM_016169.4(SUFU):c.*2140G>T rs543282016 0.00019
NM_016169.4(SUFU):c.1308C>T (p.Thr436=) rs142029957 0.00018
NM_016169.4(SUFU):c.*721T>G rs2298279 0.00014
NM_016169.4(SUFU):c.839G>A (p.Arg280Gln) rs145704867 0.00014
NM_016169.4(SUFU):c.*1451C>T rs886046659 0.00011
NM_016169.4(SUFU):c.*2195G>T rs781227748 0.00010
NM_016169.4(SUFU):c.*907C>G rs886046655 0.00008
NM_016169.4(SUFU):c.1028G>A (p.Arg343His) rs79299301 0.00008
NM_016169.4(SUFU):c.*520G>A rs757315966 0.00006
NM_016169.4(SUFU):c.992G>A (p.Arg331Gln) rs141359583 0.00005
NM_016169.4(SUFU):c.*2267G>T rs886046660 0.00004
NM_016169.4(SUFU):c.*2643C>G rs886046663 0.00003
NM_016169.4(SUFU):c.*376G>A rs866120174 0.00003
NM_016169.4(SUFU):c.*915G>C rs886046656 0.00003
NM_016169.4(SUFU):c.*1908C>G rs764234968 0.00002
NM_016169.4(SUFU):c.*3025T>C rs896765914 0.00002
NM_016169.4(SUFU):c.*844G>A rs1032441274 0.00002
NM_016169.4(SUFU):c.169A>G (p.Ile57Val) rs377614167 0.00002
NM_016169.4(SUFU):c.*1145A>G rs1190732664 0.00001
NM_016169.4(SUFU):c.*2278C>G rs530131484 0.00001
NM_016169.4(SUFU):c.*2475C>T rs886046661 0.00001
NM_016169.4(SUFU):c.*3045A>G rs185874880 0.00001
NM_016169.4(SUFU):c.*305C>A rs1430494184 0.00001
NM_016169.4(SUFU):c.*405G>A rs2063829258 0.00001
NM_016169.4(SUFU):c.180C>T (p.Tyr60=) rs776945270 0.00001
NM_016169.4(SUFU):c.183-13T>G rs749913059 0.00001
NM_016169.4(SUFU):c.529A>G (p.Met177Val) rs758672583 0.00001
NM_016169.4(SUFU):c.756+10G>C rs764838079 0.00001
NM_016169.4(SUFU):c.*1104C>T rs886046657
NM_016169.4(SUFU):c.*131C>G rs886046654
NM_016169.4(SUFU):c.*1389C>T rs886046658
NM_016169.4(SUFU):c.*138C>T rs2063826618
NM_016169.4(SUFU):c.*1690A>G rs955282121
NM_016169.4(SUFU):c.*1720C>G rs536068954
NM_016169.4(SUFU):c.*1785C>T rs1047091410
NM_016169.4(SUFU):c.*1889C>T rs139020703
NM_016169.4(SUFU):c.*2150G>A rs561461171
NM_016169.4(SUFU):c.*2479C>T rs2063847339
NM_016169.4(SUFU):c.*2553T>C rs886046662
NM_016169.4(SUFU):c.*2657T>C rs2063848688
NM_016169.4(SUFU):c.*2757G>A rs758662176
NM_016169.4(SUFU):c.*3110C>T rs141940845
NM_016169.4(SUFU):c.*3239C>G rs538132960
NM_016169.4(SUFU):c.*3239_*3241del rs767259911
NM_016169.4(SUFU):c.*352C>G rs139725961
NM_016169.4(SUFU):c.*742G>A rs142145337
NM_016169.4(SUFU):c.1022+1G>A rs587776578
NM_016169.4(SUFU):c.1174_1175dup (p.Arg393fs) rs1564707343
NM_016169.4(SUFU):c.466T>C (p.Cys156Arg) rs1554852266
NM_016169.4(SUFU):c.696C>G (p.Pro232=) rs2063434189

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