"Illumina Laboratory Services, Illumina"[submitter] AND "CYB561A3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 305046	NM_016464.4(TMEM138):c.-520_-518delTCC	CYB561A3, TMEM138	Deletion (5 prime UTR variant)	Familial aplasia of the vermis	GUncertain significance
Select item 305047	NM_016464.4(TMEM138):c.-518C>T	CYB561A3, TMEM138	Single nucleotide variant (5 prime UTR variant)	Familial aplasia of the vermis	GUncertain significance
Select item 305048	NM_016464.4(TMEM138):c.-479A>C	CYB561A3, TMEM138	Single nucleotide variant (5 prime UTR variant)	Familial aplasia of the vermis	GUncertain significance
Select item 305049	NM_016464.4(TMEM138):c.-350A>C	TMEM138, CYB561A3	Single nucleotide variant (5 prime UTR variant)	Familial aplasia of the vermis	GUncertain significance
Select item 305050	NM_016464.4(TMEM138):c.-308A>G	CYB561A3, TMEM138	Single nucleotide variant (5 prime UTR variant)	Familial aplasia of the vermis	GLikely benign
Select item 305051	NM_016464.4(TMEM138):c.-304C>A	TMEM138, CYB561A3	Single nucleotide variant (5 prime UTR variant)	Familial aplasia of the vermis	GUncertain significance
Select item 305052	NM_016464.4(TMEM138):c.-294G>A	CYB561A3, TMEM138	Single nucleotide variant (5 prime UTR variant)	Familial aplasia of the vermis	GUncertain significance

ClinVar