"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SUCLG1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 203967	NM_003849.4(SUCLG1):c.900C>T (p.Ala300=)	SUCLG1	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 3380826	NM_003849.4(SUCLG1):c.764T>C (p.Ile255Thr)	SUCLG1 (I255T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 203970	NM_003849.4(SUCLG1):c.236G>A (p.Gly79Asp)	SUCLG1 (G79D)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 559371	NM_003849.4(SUCLG1):c.98-17_98-11del	SUCLG1	Deletion (intron variant)	Mitochondrial DNA depletion syndrome 9	GLikely benign
Select item 440310	NM_003849.4(SUCLG1):c.98-14_98-11del	SUCLG1	Deletion (intron variant)	Mitochondrial DNA depletion syndrome 9 +1 more	GBenign
Select item 337162	NM_003849.4(SUCLG1):c.98-13_98-11del	SUCLG1	Deletion (intron variant)	Mitochondrial DNA depletion syndrome +2 more	GBenign
Select item 2159898	NM_003849.4(SUCLG1):c.52A>G (p.Ser18Gly)	SUCLG1 (S18G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 559372	NM_003849.4(SUCLG1):c.32T>C (p.Ile11Thr)	SUCLG1 (I11T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar