List of variants in gene SDHA reported as benign for Paragangliomas 5

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.891T>C (p.Pro297=)	rs1126417	0.74006
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.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.1752A>G (p.Ala584=)	rs13070	0.24028
NM_004168.4(SDHA):c.619A>C (p.Arg207=)	rs6555055	0.24028
NM_004168.4(SDHA):c.684T>C (p.Asn228=)	rs2115272	0.24016
NM_004168.4(SDHA):c.1969G>A (p.Val657Ile)	rs6962	0.17489
NM_004168.4(SDHA):c.1170C>T (p.Phe390=)	rs35277230	0.09677
NM_004168.4(SDHA):c.1908+15C>T	rs34504623	0.07899
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.1413C>T (p.Ile471=)	rs34779890	0.00259
NM_004168.4(SDHA):c.1623G>A (p.Lys541=)	rs35502109	0.00214
NM_004168.4(SDHA):c.1911C>T (p.Val637=)	rs11557098	0.00180
NM_004168.4(SDHA):c.163T>C (p.Tyr55His)	rs142926807	0.00078
NM_004168.4(SDHA):c.550G>A (p.Gly184Arg)	rs148246073	0.00056
NM_004168.4(SDHA):c.513T>C (p.Arg171=)	rs765157205	0.00004
NM_004168.4(SDHA):c.-28_-20dup	rs2477250587
NM_004168.4(SDHA):c.771-11A>G	rs2288461

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.