List of variants in gene SDHA reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 46

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.136A>G (p.Lys46Glu)	rs144599870	0.00145
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.600A>G (p.Leu200=)	rs201967413	0.00056
NM_004168.4(SDHA):c.456+6G>T	rs371735891	0.00047
NM_004168.4(SDHA):c.1569T>C (p.Ala523=)	rs150192376	0.00019
NM_004168.4(SDHA):c.918C>G (p.Leu306=)	rs138828792	0.00017
NM_004168.4(SDHA):c.777C>T (p.Tyr259=)	rs140243793	0.00014
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln)	rs376391115	0.00009
NM_004168.4(SDHA):c.552G>A (p.Gly184=)	rs147444427	0.00008
NM_004168.4(SDHA):c.1299C>T (p.Pro433=)	rs144473374	0.00005
NM_004168.4(SDHA):c.1014G>A (p.Ala338=)	rs201341132	0.00004
NM_004168.4(SDHA):c.1311C>T (p.Ala437=)	rs377506772	0.00004
NM_004168.4(SDHA):c.1929C>T (p.Pro643=)	rs761201589	0.00004
NM_004168.4(SDHA):c.313-7T>C	rs201972549	0.00004
NM_004168.4(SDHA):c.1215C>T (p.Thr405=)	rs762888704	0.00003
NM_004168.4(SDHA):c.1272C>T (p.His424=)	rs754805626	0.00003
NM_004168.4(SDHA):c.1629T>C (p.Tyr543=)	rs747249998	0.00003
NM_004168.4(SDHA):c.150C>T (p.Ser50=)	rs140264486	0.00002
NM_004168.4(SDHA):c.1737C>T (p.Ile579=)	rs201454617	0.00002
NM_004168.4(SDHA):c.1755G>A (p.Arg585=)	rs760254364	0.00002
NM_004168.4(SDHA):c.1799G>A (p.Arg600Gln)	rs1126568	0.00002
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.1371C>A (p.Leu457=)	rs75091805	0.00001
NM_004168.4(SDHA):c.1734C>G (p.Thr578=)	rs748328205	0.00001
NM_004168.4(SDHA):c.1923T>C (p.Tyr641=)	rs1444319863	0.00001
NM_004168.4(SDHA):c.429G>A (p.Thr143=)	rs906281170	0.00001
NM_004168.4(SDHA):c.477G>A (p.Pro159=)	rs771741537	0.00001
NM_004168.4(SDHA):c.895+8A>G	rs892273080	0.00001
NM_004168.4(SDHA):c.*9G>C
NM_004168.4(SDHA):c.1038C>T (p.Ser346=)	rs1041949
NM_004168.4(SDHA):c.1119A>G (p.Pro373=)	rs1428505412
NM_004168.4(SDHA):c.1332C>G (p.Ala444=)	rs1060505011
NM_004168.4(SDHA):c.1335G>T (p.Ser445=)	rs200223188
NM_004168.4(SDHA):c.1378C>T (p.Leu460=)	rs760686493
NM_004168.4(SDHA):c.1433-8dup	rs769594966
NM_004168.4(SDHA):c.1664-4C>G	rs774876028
NM_004168.4(SDHA):c.1812C>T (p.Tyr604=)	rs1436919553
NM_004168.4(SDHA):c.1848G>A (p.Lys616=)
NM_004168.4(SDHA):c.1857G>A (p.Glu619=)	rs1247081812
NM_004168.4(SDHA):c.1908+8T>G	rs2126641731
NM_004168.4(SDHA):c.1908+9G>A	rs767578208
NM_004168.4(SDHA):c.1909-12_1909-11del	rs372662724
NM_004168.4(SDHA):c.891T>G (p.Pro297=)	rs1126417
NM_004168.4(SDHA):c.999C>G (p.Val333=)	rs149556555

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.