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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042773	NM_003006.4(SELPLG):c.1005C>T (p.Phe335=)	SELPLG	Single nucleotide variant (synonymous variant)	SELPLG-related disorder	GLikely benign
Select item 3057867	NM_003006.4(SELPLG):c.913G>A (p.Val305Ile)	SELPLG (V305I +1 more)	Single nucleotide variant (missense variant)	SELPLG-related disorder	GLikely benign
Select item 756589	NM_003006.4(SELPLG):c.912C>T (p.Ser304=)	SELPLG	Single nucleotide variant (synonymous variant)	SELPLG-related disorder +1 more	GLikely benign
Select item 3035787	NM_003006.4(SELPLG):c.324C>T (p.Asn108=)	SELPLG	Single nucleotide variant (synonymous variant)	SELPLG-related disorder	GLikely benign
Select item 3055988	NM_003006.4(SELPLG):c.186G>A (p.Met62Ile)	SELPLG (M62I +1 more)	Single nucleotide variant (missense variant)	SELPLG-related disorder	GBenign
Select item 3044050	NM_003006.4(SELPLG):c.132C>T (p.Thr44=)	SELPLG	Single nucleotide variant (synonymous variant)	SELPLG-related disorder	GLikely benign

ClinVar