ClinVar Miner

List of variants in gene SDHA reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
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Total variants: 34
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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.895+28T>C rs2288459 0.25210
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.1664-34C>T rs10041187 0.25155
NM_004168.4(SDHA):c.896-20A>G rs7710005 0.25110
NM_004168.4(SDHA):c.1432+39C>T rs10057677 0.24939
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.896-32G>A rs7725241 0.10356
NM_004168.4(SDHA):c.456+32G>A rs35464369 0.10345
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_004168.4(SDHA):c.456+20G>C rs193283468 0.00385
NM_004168.4(SDHA):c.313-19G>T rs185555941 0.00235
NM_004168.4(SDHA):c.1911C>T (p.Val637=) rs11557098 0.00180
NM_004168.4(SDHA):c.723C>T (p.Asp241=) rs146653693 0.00049
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter) rs142441643 0.00025
NM_004168.4(SDHA):c.553C>T (p.Gln185Ter) rs775827529 0.00001
NM_004168.4(SDHA):c.-7A>C rs751633537
NM_004168.4(SDHA):c.168del (p.Pro56_Val57insTer)
NM_004168.4(SDHA):c.622-7C>T rs759371428
NM_004168.4(SDHA):c.771-11A>G rs2288461

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