"PreventionGenetics, part of Exact Sciences"[submitter] AND "PRRG4"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059407	NM_024081.6(PRRG4):c.97G>A (p.Glu33Lys)	PRRG4 (E33K)	Single nucleotide variant (missense variant)	PRRG4-related disorder	GBenign
Select item 3056859	NM_024081.6(PRRG4):c.103+8C>T	PRRG4	Single nucleotide variant (intron variant)	PRRG4-related disorder	GBenign
Select item 3040286	NM_024081.6(PRRG4):c.451T>A (p.Ser151Thr)	PRRG4 (S151T)	Single nucleotide variant (missense variant)	PRRG4-related disorder	GLikely benign
Select item 3040547	NM_024081.6(PRRG4):c.452C>A (p.Ser151Tyr)	PRRG4 (S151Y)	Single nucleotide variant (missense variant)	PRRG4-related disorder	GLikely benign
Select item 3056875	NM_024081.6(PRRG4):c.527C>A (p.Pro176Gln)	PRRG4 (P176Q)	Single nucleotide variant (missense variant)	PRRG4-related disorder	GBenign
Select item 3058902	NM_024081.6(PRRG4):c.534G>A (p.Pro178=)	PRRG4	Single nucleotide variant (synonymous variant)	PRRG4-related disorder	GBenign

ClinVar