"Invitae"[submitter] AND "PYGB"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718469	NM_002862.4(PYGB):c.170C>G (p.Ala57Gly)	PYGB (A57G)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 713733	NM_002862.4(PYGB):c.540C>T (p.Ala180=)	PYGB	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 769084	NM_002862.4(PYGB):c.1245G>A (p.Val415=)	PYGB	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 735387	NM_002862.4(PYGB):c.1977G>A (p.Pro659=)	PYGB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 713734	NM_002862.4(PYGB):c.2312+9G>A	PYGB	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2423578	NC_000020.10:g.(?_25056897)_(25320007_?)dup	ABHD12, ENTPD6 +2 more	Duplication	not provided	GUncertain significance

ClinVar