ClinVar Miner

List of variants studied for central nervous system cancer by KCCC/NGS Laboratory, Kuwait Cancer Control Center

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 50
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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_004168.4(SDHA):c.891T>C (p.Pro297=) rs1126417 0.74998
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_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_004168.4(SDHA):c.113A>T (p.Asp38Val) rs34635677 0.02888
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_004168.4(SDHA):c.822C>T (p.Gly274=) rs34771391 0.01114
NM_004168.4(SDHA):c.549C>T (p.Gly183=) rs61733344 0.00892
NM_004168.4(SDHA):c.969C>T (p.Gly323=) rs142849100 0.00430
NM_003000.3(SDHB):c.-37T>C rs143031690 0.00411
NM_004168.4(SDHA):c.456+20G>C rs193283468 0.00385
NM_004168.4(SDHA):c.1413C>T (p.Ile471=) rs34779890 0.00259
NM_004168.4(SDHA):c.313-19G>T rs185555941 0.00235
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_004168.4(SDHA):c.1368G>A (p.Ser456=) rs149875171 0.00117
NM_004168.4(SDHA):c.1002G>A (p.Ala334=) rs144252500 0.00075
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.113G>A (p.Arg38His) rs143058777 0.00010
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln) rs376391115 0.00009
NM_003000.3(SDHB):c.765+13G>A rs115561881 0.00002
NM_004168.4(SDHA):c.1737C>T (p.Ile579=) rs201454617 0.00002
NM_004168.4(SDHA):c.1765C>T (p.Arg589Trp) rs387906780 0.00002
NM_003000.3(SDHB):c.143A>T (p.Asp48Val) rs202101384 0.00001
NM_003000.3(SDHB):c.700C>T (p.Leu234=) rs201728852 0.00001
NM_004168.4(SDHA):c.1182C>T (p.Asp394=) rs377317558 0.00001
NM_004168.4(SDHA):c.1308C>T (p.Tyr436=) rs762494024 0.00001
NM_004168.4(SDHA):c.1323C>T (p.Ala441=) rs751561561 0.00001
NM_004168.4(SDHA):c.1410C>T (p.Ser470=) rs556476038 0.00001
NM_004168.4(SDHA):c.1754G>A (p.Arg585Gln) rs752360961 0.00001
NM_004168.4(SDHA):c.896-4G>A rs555881974 0.00001
NM_003000.3(SDHB):c.598dup (p.Trp200fs) rs2101516417
NM_004168.4(SDHA):c.771-11A>G rs2288461

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