List of variants in gene SUCLA2 reported as benign for Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_003850.3(SUCLA2):c.*217T>C	rs4941618	0.93675
NM_003850.3(SUCLA2):c.595T>A (p.Ser199Thr)	rs7320366	0.79365
NM_003850.3(SUCLA2):c.371+9C>T	rs6561424	0.72762
NM_003850.3(SUCLA2):c.*328A>G	rs13243	0.08452
NM_003850.3(SUCLA2):c.*661C>A	rs10397	0.07143
NM_003850.3(SUCLA2):c.110T>G (p.Leu37Trp)	rs62636645	0.02383
NM_003850.3(SUCLA2):c.510A>G (p.Ala170=)	rs35568795	0.01320
NM_003850.3(SUCLA2):c.1099G>A (p.Asp367Asn)	rs117412559	0.00951
NM_003850.3(SUCLA2):c.*581T>G	rs74615692	0.00652
NM_003850.3(SUCLA2):c.256A>G (p.Ile86Val)	rs61756204	0.00451
NM_003850.3(SUCLA2):c.789T>C (p.Asp263=)	rs57270175	0.00441
NM_003850.3(SUCLA2):c.811A>G (p.Met271Val)	rs142020748	0.00221
NM_003850.2(SUCLA2):c.-34G>T	rs373530187	0.00059
NM_003850.3(SUCLA2):c.*205T>C	rs149321505	0.00058
NM_003850.3(SUCLA2):c.660C>T (p.Leu220=)	rs148794726	0.00051
NM_003850.3(SUCLA2):c.1074A>C (p.Thr358=)	rs746516356	0.00004
NM_003850.3(SUCLA2):c.*661C>G	rs10397

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