"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZBTB11"[g - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043173	NM_014415.4(ZBTB11):c.10_13del	ZBTB11	Deletion (3 prime UTR variant)	ZBTB11-related disorder	GLikely benign
Select item 3047351	NM_014415.4(ZBTB11):c.2760C>T (p.Ser920=)	ZBTB11	Single nucleotide variant (synonymous variant)	ZBTB11-related disorder	GLikely benign
Select item 3060760	NM_014415.4(ZBTB11):c.2645-4_2645-3del	ZBTB11	Deletion (intron variant)	ZBTB11-related disorder	GLikely benign
Select item 3038505	NM_014415.4(ZBTB11):c.2268A>G (p.Lys756=)	ZBTB11	Single nucleotide variant (synonymous variant)	ZBTB11-related disorder	GLikely benign
Select item 3043402	NM_014415.4(ZBTB11):c.2214A>G (p.Ser738=)	ZBTB11	Single nucleotide variant (synonymous variant)	ZBTB11-related disorder	GLikely benign
Select item 3049773	NM_014415.4(ZBTB11):c.1719A>G (p.Glu573=)	ZBTB11	Single nucleotide variant (synonymous variant)	ZBTB11-related disorder	GLikely benign
Select item 1695079	NM_014415.4(ZBTB11):c.1345A>T (p.Ser449Cys)	ZBTB11 (S449C)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3041119	NM_014415.4(ZBTB11):c.1145G>A (p.Arg382Gln)	ZBTB11 (R382Q)	Single nucleotide variant (missense variant)	ZBTB11-related disorder	GLikely benign
Select item 3055253	NM_014415.4(ZBTB11):c.219C>T (p.Asp73=)	ZBTB11, ZBTB11-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	ZBTB11-related disorder	GLikely benign