ClinVar Miner

List of variants reported as uncertain significance for brain neoplasm by Illumina Laboratory Services, Illumina

Included ClinVar conditions (50):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
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.*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.50C>T (p.Ala17Val) rs12780580 0.00023
NM_016169.4(SUFU):c.*1997A>G rs757368847 0.00021
NM_016169.4(SUFU):c.6G>T (p.Ala2=) rs746555296 0.00021
NM_016169.4(SUFU):c.1445C>T (p.Pro482Leu) rs765358771 0.00020
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_003977.4(AIP):c.166C>T (p.Arg56Cys) rs267606538 0.00001
NM_003977.4(AIP):c.174G>C (p.Lys58Asn) rs267606539 0.00001
NM_003977.4(AIP):c.468+3G>A rs868823652 0.00001
NM_003977.4(AIP):c.944A>C (p.Gln315Pro) rs886048585 0.00001
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_003977.4(AIP):c.-12C>G rs551077555
NM_003977.4(AIP):c.-2G>C rs377710724
NM_003977.4(AIP):c.-85C>T rs1565180279
NM_003977.4(AIP):c.102C>G (p.Ala34=) rs886048584
NM_003977.4(AIP):c.249G>A (p.Gly83=) rs104895072
NM_003977.4(AIP):c.379A>G (p.Met127Val) rs1591044815
NM_003977.4(AIP):c.660C>T (p.Ser220=) rs776495655
NM_016169.3(SUFU):c.-189C>T rs1589969363
NM_016169.3(SUFU):c.-202C>T rs1222242003
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.*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.-103C>A rs886046653
NM_016169.4(SUFU):c.-163A>G rs886046652
NM_016169.4(SUFU):c.-181A>G rs867202826
NM_016169.4(SUFU):c.-81C>A rs546107381
NM_016169.4(SUFU):c.-81C>T rs546107381
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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