"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC1A4"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 624135	NM_003038.5(SLC1A4):c.65C>T (p.Pro22Leu)	SLC1A4 (P22L)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3030663	NM_003038.5(SLC1A4):c.177C>A (p.Gly59=)	SLC1A4	Single nucleotide variant (synonymous variant +1 more)	SLC1A4-related disorder	GLikely benign
Select item 1165648	NM_003038.5(SLC1A4):c.234C>G (p.Pro78=)	SLC1A4	Single nucleotide variant (synonymous variant +1 more)	SLC1A4-related disorder +1 more	GBenign/Likely benign
Select item 2632949	NM_003038.5(SLC1A4):c.634-1G>C	SLC1A4	Single nucleotide variant (splice acceptor variant)	SLC1A4-related disorder	GLikely pathogenic
Select item 736001	NM_003038.5(SLC1A4):c.999C>T (p.Leu333=)	SLC1A4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 762126	NM_003038.5(SLC1A4):c.1041G>A (p.Ala347=)	SLC1A4	Single nucleotide variant (synonymous variant)	SLC1A4-related disorder +1 more	GLikely benign
Select item 786483	NM_003038.5(SLC1A4):c.1313T>C (p.Ile438Thr)	SLC1A4 (I218T +2 more)	Single nucleotide variant (missense variant)	SLC1A4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1170081	NM_003038.5(SLC1A4):c.1590G>A (p.Ser530=)	SLC1A4	Single nucleotide variant (synonymous variant)	SLC1A4-related disorder +1 more	GBenign

ClinVar