List of variants in gene SUCLG1 reported as likely benign by GeneDx

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_003849.4(SUCLG1):c.202-65G>C	rs58623633	0.01199
NM_003849.4(SUCLG1):c.97+60A>G	rs111529460	0.01198
NM_003849.4(SUCLG1):c.318+107T>C	rs60175463	0.01121
NM_003849.4(SUCLG1):c.*55G>C	rs80166442	0.01010
NM_003849.4(SUCLG1):c.*207A>G	rs73942653	0.00784
NM_003849.4(SUCLG1):c.318+174G>T	rs147130548	0.00738
NM_003849.4(SUCLG1):c.318+197G>A	rs143558184	0.00334
NM_003849.4(SUCLG1):c.825+18A>G	rs143229361	0.00323
NM_003849.4(SUCLG1):c.589+219G>A	rs148771299	0.00205
NM_003849.4(SUCLG1):c.291C>T (p.Gly97=)	rs35996428	0.00183
NM_003849.4(SUCLG1):c.384C>T (p.Ala128=)	rs139731592	0.00048
NM_003849.4(SUCLG1):c.97+17C>T	rs113923257	0.00032
NM_003849.4(SUCLG1):c.345T>C (p.Ala115=)	rs374594774	0.00027
NM_003849.4(SUCLG1):c.63C>A (p.Leu21=)	rs982734922	0.00012
NM_003849.4(SUCLG1):c.102G>A (p.Pro34=)	rs767975978	0.00011
NM_003849.4(SUCLG1):c.590-6G>A	rs200107730	0.00008
NM_003849.3(SUCLG1):c.-15G>A	rs779839691	0.00006
NM_003849.4(SUCLG1):c.590-7C>T	rs537348295	0.00005
NM_003849.4(SUCLG1):c.826-8del	rs1176620455	0.00003
NM_003849.4(SUCLG1):c.202-18T>C	rs1343564047	0.00001
NM_003849.4(SUCLG1):c.402G>A (p.Glu134=)	rs1672770354	0.00001
NM_003849.4(SUCLG1):c.502A>G (p.Ile168Val)	rs763324017	0.00001
NM_003849.4(SUCLG1):c.318+233G>A	rs79101523
NM_003849.4(SUCLG1):c.531+9dup	rs769785912
NM_003849.4(SUCLG1):c.826-13_826-10del	rs1064793276

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