ClinVar Miner

List of variants reported as benign for central nervous system neoplasm by KCCC/NGS Laboratory, Kuwait Cancer Control Center

Included ClinVar conditions (115):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_003000.3(SDHB):c.201-36G>T rs1022580 0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=) rs2746462 0.95374
NM_003977.4(AIP):c.682C>A (p.Gln228Lys) rs641081 0.84113
NM_004168.4(SDHA):c.891T>C (p.Pro297=) rs1126417 0.74998
NM_016169.4(SUFU):c.1365+19T>C rs12414407 0.68248
NM_016169.4(SUFU):c.182+16C>T rs2274351 0.46492
NM_004168.4(SDHA):c.1932G>A (p.Val644=) rs6961 0.26598
NM_004168.4(SDHA):c.1038C>G (p.Ser346=) rs1041949 0.26134
NM_004168.4(SDHA):c.619A>C (p.Arg207=) rs6555055 0.25190
NM_004168.4(SDHA):c.1752A>G (p.Ala584=) rs13070 0.25187
NM_004168.4(SDHA):c.684T>C (p.Asn228=) rs2115272 0.25174
NM_004168.4(SDHA):c.309A>G (p.Ala103=) rs1139424 0.25161
NM_004168.4(SDHA):c.1680G>A (p.Thr560=) rs1139449 0.25156
NM_004168.4(SDHA):c.896-20A>G rs7710005 0.25110
NM_004168.4(SDHA):c.1886A>T (p.Tyr629Phe) rs6960 0.24550
NM_004168.4(SDHA):c.1969G>A (p.Val657Ile) rs6962 0.18133
NM_016169.4(SUFU):c.1299T>C (p.Ile433=) rs17114803 0.14628
NM_003002.4(SDHD):c.315-32T>C rs4151637 0.11444
NM_003002.4(SDHD):c.170-29A>G rs9919624 0.11431
NM_003002.4(SDHD):c.204C>T (p.Ser68=) rs9919552 0.11428
NM_003000.3(SDHB):c.200+33G>A rs2647169 0.10785
NM_004168.4(SDHA):c.1170C>T (p.Phe390=) rs35277230 0.10356
NM_004168.4(SDHA):c.1908+15C>T rs34504623 0.08152
NM_003977.4(AIP):c.516C>T (p.Asp172=) rs2276020 0.03152
NM_004168.4(SDHA):c.113A>T (p.Asp38Val) rs34635677 0.02888
NM_003977.4(AIP):c.132C>T (p.Asp44=) rs11822907 0.02357
NM_003001.5(SDHC):c.-38G>A rs112556972 0.01611
NM_004168.4(SDHA):c.1664-8G>A rs199790689 0.01533
NM_004168.4(SDHA):c.1305G>T (p.Leu435=) rs35964044 0.01515
NM_004168.4(SDHA):c.1776T>C (p.His592=) rs1126538 0.01372
NM_003001.5(SDHC):c.-32T>C rs115782155 0.01342
NM_004168.4(SDHA):c.822C>T (p.Gly274=) rs34771391 0.01114
NM_004168.4(SDHA):c.549C>T (p.Gly183=) rs61733344 0.00892
NM_003002.4(SDHD):c.312C>T (p.His104=) rs61734352 0.00690
NM_003001.5(SDHC):c.354T>C (p.Phe118=) rs61733156 0.00454
NM_004168.4(SDHA):c.969C>T (p.Gly323=) rs142849100 0.00430
NM_004168.4(SDHA):c.456+20G>C rs193283468 0.00385
NM_004168.4(SDHA):c.1413C>T (p.Ile471=) rs34779890 0.00259
NM_003000.3(SDHB):c.170A>G (p.His57Arg) rs35962811 0.00231
NM_004168.4(SDHA):c.1623G>A (p.Lys541=) rs35502109 0.00206
NM_004168.4(SDHA):c.1911C>T (p.Val637=) rs11557098 0.00180
NM_003000.3(SDHB):c.300T>C (p.Ser100=) rs11541235 0.00157
NM_016169.4(SUFU):c.600C>T (p.Ile200=) rs149513330 0.00116
NM_004168.4(SDHA):c.550G>A (p.Gly184Arg) rs148246073 0.00056
NM_004168.4(SDHA):c.163T>C (p.Tyr55His) rs142926807 0.00046
NM_003000.3(SDHB):c.765+13G>A rs115561881 0.00002
NM_016169.4(SUFU):c.645C>T (p.Asn215=) rs551772204 0.00001
NM_004168.4(SDHA):c.771-11A>G rs2288461

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