ClinVar Miner

List of variants in gene SUFU reported as benign for brain disorder

Included ClinVar conditions (1840):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_016169.4(SUFU):c.1365+19T>C rs12414407 0.68248
NM_016169.4(SUFU):c.182+16C>T rs2274351 0.46492
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.*118C>T rs2298277 0.00835
NM_016169.4(SUFU):c.1018G>T (p.Ala340Ser) rs34135067 0.00646
NM_016169.4(SUFU):c.1291T>C (p.Leu431=) rs141950577 0.00487
NM_016169.4(SUFU):c.210T>C (p.Tyr70=) rs35166585 0.00430
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.1308C>T (p.Thr436=) rs142029957 0.00018
NM_016169.4(SUFU):c.1245C>T (p.Gly415=) rs144158469 0.00011
NM_016169.4(SUFU):c.183-4G>A rs766044613 0.00005
NM_016169.4(SUFU):c.911-16A>C rs777832144 0.00002
NM_016169.4(SUFU):c.645C>T (p.Asn215=) rs551772204 0.00001

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