ClinVar Miner

List of variants in gene SDHA reported as benign for central nervous system neoplasm

Included ClinVar conditions (115):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
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_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.17G>A (p.Gly6Asp) rs187964306 0.00596
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.146A>G (p.Asp49Gly) rs80207011 0.00261
NM_004168.4(SDHA):c.1413C>T (p.Ile471=) rs34779890 0.00259
NM_004168.4(SDHA):c.1523C>T (p.Thr508Ile) rs151266052 0.00245
NM_004168.4(SDHA):c.313-19G>T rs185555941 0.00235
NM_004168.4(SDHA):c.1623G>A (p.Lys541=) rs35502109 0.00206
NM_004168.4(SDHA):c.1551+16C>T rs184954254 0.00198
NM_004168.4(SDHA):c.1911C>T (p.Val637=) rs11557098 0.00180
NM_004168.4(SDHA):c.1368G>A (p.Ser456=) rs149875171 0.00117
NM_004168.4(SDHA):c.1396G>A (p.Ala466Thr) rs111387770 0.00097
NM_004168.4(SDHA):c.1260+13G>T rs185239026 0.00076
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.723C>T (p.Asp241=) rs146653693 0.00049
NM_004168.4(SDHA):c.163T>C (p.Tyr55His) rs142926807 0.00046
NM_004168.4(SDHA):c.1569T>C (p.Ala523=) rs150192376 0.00019
NM_004168.4(SDHA):c.1089C>T (p.His363=) rs368488126 0.00008
NM_004168.4(SDHA):c.513T>C (p.Arg171=) rs765157205 0.00004
NM_004168.4(SDHA):c.1394G>A (p.Arg465Gln) rs138277996 0.00002
NM_004168.4(SDHA):c.1367C>T (p.Ser456Leu) rs76896145 0.00001
NM_004168.4(SDHA):c.1371C>A (p.Leu457=) rs75091805 0.00001
NM_004168.4(SDHA):c.-28_-20dup
NM_004168.4(SDHA):c.1260+23dup
NM_004168.4(SDHA):c.1432+20G>C rs200127852
NM_004168.4(SDHA):c.1433-3del rs2126602411
NM_004168.4(SDHA):c.1433-8del
NM_004168.4(SDHA):c.1433-8dup rs769594966
NM_004168.4(SDHA):c.150+17dup rs1734837730
NM_004168.4(SDHA):c.1664-11del rs1561010692
NM_004168.4(SDHA):c.457-12del rs2126549133
NM_004168.4(SDHA):c.771-11A>G rs2288461
NM_004168.4(SDHA):c.896-5del rs751123858

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