"Genetic Services Laboratory, University of Chicago"[submitter] AND "R - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1336843	NM_001014.5(RPS10):c.444C>T (p.Thr148=)	RPS10, RPS10-NUDT3	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 356419	NM_001014.5(RPS10):c.408C>T (p.Ala136=)	RPS10-NUDT3, RPS10	Single nucleotide variant (synonymous variant)	RPS10-NUDT3-related disorder +5 more	GBenign/Likely benign
Select item 1337957	NM_001014.5(RPS10):c.292dup (p.Arg98fs)	RPS10, RPS10-NUDT3 (R98fs)	Duplication (frameshift variant)	not provided	GLikely pathogenic
Select item 463371	NM_001014.5(RPS10):c.261G>A (p.Pro87=)	RPS10, RPS10-NUDT3	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 238211	NM_001014.5(RPS10):c.231G>A (p.Gln77=)	RPS10, RPS10-NUDT3	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 463370	NM_001014.5(RPS10):c.204C>T (p.Tyr68=)	RPS10-NUDT3, RPS10	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 9 +3 more	GBenign/Likely benign

ClinVar