ClinVar Miner

List of variants in gene SDHA studied for Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Total variants: 67
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HGVS dbSNP
NM_004168.4(SDHA):c.*102G>A
NM_004168.4(SDHA):c.*133G>C rs193112615
NM_004168.4(SDHA):c.*179G>A
NM_004168.4(SDHA):c.*189C>T rs185107377
NM_004168.4(SDHA):c.*249T>C
NM_004168.4(SDHA):c.*75A>G rs886060517
NM_004168.4(SDHA):c.-1C>T rs560932680
NM_004168.4(SDHA):c.-2A>T rs763680697
NM_004168.4(SDHA):c.-4A>G rs377134185
NM_004168.4(SDHA):c.-7A>C rs751633537
NM_004168.4(SDHA):c.1002G>A (p.Ala334=) rs144252500
NM_004168.4(SDHA):c.1014G>A (p.Ala338=) rs201341132
NM_004168.4(SDHA):c.1038C>G (p.Ser346=) rs1041949
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln) rs199844384
NM_004168.4(SDHA):c.1092C>T (p.Val364=) rs886060515
NM_004168.4(SDHA):c.113A>T (p.Asp38Val) rs34635677
NM_004168.4(SDHA):c.1170C>T (p.Phe390=) rs35277230
NM_004168.4(SDHA):c.1177G>A (p.Val393Met) rs372989971
NM_004168.4(SDHA):c.1188G>A (p.Thr396=) rs778667374
NM_004168.4(SDHA):c.1305G>T (p.Leu435=) rs35964044
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr) rs140736646
NM_004168.4(SDHA):c.1368G>A (p.Ser456=) rs149875171
NM_004168.4(SDHA):c.1413C>T (p.Ile471=) rs34779890
NM_004168.4(SDHA):c.1527G>A (p.Ser509=) rs746453879
NM_004168.4(SDHA):c.1580G>A (p.Arg527His) rs766352407
NM_004168.4(SDHA):c.1623G>A (p.Lys541=) rs35502109
NM_004168.4(SDHA):c.163T>C (p.Tyr55His) rs142926807
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln) rs376391115
NM_004168.4(SDHA):c.1664-8G>A rs199790689
NM_004168.4(SDHA):c.1680G>A (p.Thr560=) rs1139449
NM_004168.4(SDHA):c.1725G>A (p.Ala575=) rs758252610
NM_004168.4(SDHA):c.1727T>C (p.Leu576Pro) rs1318046349
NM_004168.4(SDHA):c.1752A>G (p.Ala584=) rs13070
NM_004168.4(SDHA):c.1776T>C (p.His592=) rs1126538
NM_004168.4(SDHA):c.17G>A (p.Gly6Asp) rs187964306
NM_004168.4(SDHA):c.1886A>T (p.Tyr629Phe) rs6960
NM_004168.4(SDHA):c.1908+15C>T rs34504623
NM_004168.4(SDHA):c.1911C>T (p.Val637=) rs11557098
NM_004168.4(SDHA):c.1932G>A (p.Val644=) rs6961
NM_004168.4(SDHA):c.1969G>A (p.Val657Ile) rs6962
NM_004168.4(SDHA):c.1969G>C (p.Val657Leu)
NM_004168.4(SDHA):c.1973C>T (p.Pro658Leu) rs377632619
NM_004168.4(SDHA):c.1974G>C (p.Pro658=) rs1042446
NM_004168.4(SDHA):c.1977A>G (p.Pro659=) rs768693502
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly) rs191412461
NM_004168.4(SDHA):c.269T>C (p.Val90Ala) rs886060514
NM_004168.4(SDHA):c.309A>G (p.Ala103=) rs1139424
NM_004168.4(SDHA):c.403G>A (p.Asp135Asn)
NM_004168.4(SDHA):c.441C>T (p.Pro147=) rs201453889
NM_004168.4(SDHA):c.442G>A (p.Ala148Thr) rs375576259
NM_004168.4(SDHA):c.512G>A (p.Arg171His) rs587782076
NM_004168.4(SDHA):c.549C>T (p.Gly183=) rs61733344
NM_004168.4(SDHA):c.550G>A (p.Gly184Arg) rs148246073
NM_004168.4(SDHA):c.558C>T (p.Ala186=) rs199618059
NM_004168.4(SDHA):c.583C>T (p.Arg195Trp)
NM_004168.4(SDHA):c.5C>T (p.Ser2Leu) rs780064103
NM_004168.4(SDHA):c.619A>C (p.Arg207=) rs6555055
NM_004168.4(SDHA):c.684T>C (p.Asn228=) rs2115272
NM_004168.4(SDHA):c.723C>T (p.Asp241=) rs146653693
NM_004168.4(SDHA):c.771-11A>G rs2288461
NM_004168.4(SDHA):c.777C>T (p.Tyr259=) rs140243793
NM_004168.4(SDHA):c.822C>T (p.Gly274=) rs34771391
NM_004168.4(SDHA):c.830C>T (p.Thr277Met) rs367721665
NM_004168.4(SDHA):c.891T>C (p.Pro297=) rs1126417
NM_004168.4(SDHA):c.895+13G>A rs201461936
NM_004168.4(SDHA):c.896-11G>T
NM_004168.4(SDHA):c.969C>T (p.Gly323=) rs142849100

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