List of variants in gene SDHA reported as likely benign for not specified

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: 45

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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.1969G>A (p.Val657Ile)	rs6962	0.18133
NM_004168.4(SDHA):c.1170C>T (p.Phe390=)	rs35277230	0.10356
NM_004168.4(SDHA):c.1664-8G>A	rs199790689	0.01533
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.136A>G (p.Lys46Glu)	rs144599870	0.00145
NM_004168.4(SDHA):c.1368G>A (p.Ser456=)	rs149875171	0.00117
NM_004168.4(SDHA):c.1065-43G>A	rs193132294	0.00111
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.133G>A (p.Ala45Thr)	rs140736646	0.00060
NM_004168.4(SDHA):c.723C>T (p.Asp241=)	rs146653693	0.00049
NM_004168.4(SDHA):c.895+13G>A	rs201461936	0.00025
NM_004168.4(SDHA):c.1569T>C (p.Ala523=)	rs150192376	0.00019
NM_004168.4(SDHA):c.1552-15T>C	rs543628983	0.00014
NM_004168.4(SDHA):c.621+16T>C	rs769390635	0.00011
NM_004168.4(SDHA):c.1089C>T (p.His363=)	rs368488126	0.00008
NM_004168.4(SDHA):c.770+12A>G	rs201245536	0.00007
NM_004168.4(SDHA):c.456+9C>T	rs200565489	0.00004
NM_004168.4(SDHA):c.513T>C (p.Arg171=)	rs765157205	0.00004
NM_004168.4(SDHA):c.705C>T (p.Ile235=)	rs549892491	0.00004
NM_004168.4(SDHA):c.1233C>T (p.Gly411=)	rs376530094	0.00003
NM_004168.4(SDHA):c.1356C>T (p.Leu452=)	rs748496836	0.00002
NM_004168.4(SDHA):c.1551+4A>G	rs928294715	0.00001
NM_004168.4(SDHA):c.1664-13T>C	rs1057524514	0.00001
NM_004168.4(SDHA):c.1971C>T (p.Val657=)	rs746083858	0.00001
NM_004168.4(SDHA):c.*15G>A	rs1057522224
NM_004168.4(SDHA):c.-7A>C	rs751633537
NM_004168.4(SDHA):c.1038C>T (p.Ser346=)	rs1041949
NM_004168.4(SDHA):c.1293T>C (p.Ile431=)	rs1553999716
NM_004168.4(SDHA):c.1908+16G>C
NM_004168.4(SDHA):c.1909-12_1909-11del	rs372662724
NM_004168.4(SDHA):c.1974G>C (p.Pro658=)	rs1042446
NM_004168.4(SDHA):c.453C>T (p.Val151=)	rs138917116
NM_004168.4(SDHA):c.63+19C>A	rs1553996384
NM_004168.4(SDHA):c.84A>G (p.Thr28=)	rs1553997162

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