"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TMEM132 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 739691	NM_133448.3(TMEM132D):c.3255C>T (p.Cys1085=)	TMEM132D	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 773268	NM_133448.3(TMEM132D):c.3183C>T (p.Thr1061=)	TMEM132D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778670	NM_133448.3(TMEM132D):c.2492C>T (p.Ser831Leu)	TMEM132D (S831L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 774330	NM_133448.3(TMEM132D):c.1661A>G (p.Asp554Gly)	TMEM132D (D554G)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 715033	NM_133448.3(TMEM132D):c.1434C>T (p.Asp478=)	TMEM132D, TMEM132D-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 787103	NM_133448.3(TMEM132D):c.1302G>A (p.Glu434=)	TMEM132D, TMEM132D-AS2	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 725627	NM_133448.3(TMEM132D):c.729C>T (p.Asp243=)	TMEM132D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791366	NM_133448.3(TMEM132D):c.354A>G (p.Gly118=)	TMEM132D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780153	NM_133448.3(TMEM132D):c.269T>A (p.Leu90Gln)	TMEM132D (L90Q)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar