"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC38A10" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034657	NM_001037984.3(SLC38A10):c.3065T>C (p.Leu1022Pro)	SLC38A10 (L1022P)	Single nucleotide variant (missense variant)	SLC38A10-related disorder	GLikely benign
Select item 3037674	NM_001037984.3(SLC38A10):c.2779A>G (p.Lys927Glu)	SLC38A10 (K927E)	Single nucleotide variant (missense variant)	SLC38A10-related disorder	GLikely benign
Select item 3050225	NM_001037984.3(SLC38A10):c.2065+253G>A	SLC38A10 (R773H)	Single nucleotide variant (missense variant +1 more)	SLC38A10-related disorder	GLikely benign
Select item 3041712	NM_001037984.3(SLC38A10):c.2065+54C>T	SLC38A10 (L707F)	Single nucleotide variant (missense variant +1 more)	SLC38A10-related disorder	GLikely benign
Select item 3031872	NM_001037984.3(SLC38A10):c.2010C>T (p.Arg670=)	SLC38A10	Single nucleotide variant (synonymous variant)	SLC38A10-related disorder	GLikely benign
Select item 3038381	NM_001037984.3(SLC38A10):c.1146C>T (p.Val382=)	SLC38A10	Single nucleotide variant (synonymous variant)	SLC38A10-related disorder	GBenign

ClinVar