"PreventionGenetics, part of Exact Sciences"[submitter] AND "TUSC3"[ge - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042339	NM_006765.4(TUSC3):c.15C>A (p.Gly5=)	TUSC3	Single nucleotide variant (synonymous variant +3 more)	TUSC3-related disorder	GLikely benign
Select item 130692	NM_006765.4(TUSC3):c.193A>G (p.Ile65Val)	TUSC3 (I65V)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 95430	NM_006765.4(TUSC3):c.309-6T>C	TUSC3	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 95431	NM_006765.4(TUSC3):c.912G>A (p.Ser304=)	TUSC3	Single nucleotide variant (synonymous variant)	Intellectual disability, autosomal recessive 7 +5 more	GBenign/Likely benign
Select item 130691	NM_006765.4(TUSC3):c.1028+8C>G	TUSC3	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign

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