C5561938[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1699050	NM_030912.3(TRIM8):c.1257C>A (p.Cys419Ter)	TRIM8 (C387* +1 more)	Single nucleotide variant (nonsense +1 more)	Focal segmental glomerulosclerosis and neurodevelopmental syndrome	GPathogenic
Select item 1805889	NM_030912.3(TRIM8):c.1357C>T (p.Gln453Ter)	TRIM8 (Q421* +1 more)	Single nucleotide variant (nonsense +1 more)	Focal segmental glomerulosclerosis and neurodevelopmental syndrome	GPathogenic