"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "SP - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 262666	NM_152594.3(SPRED1):c.207+37A>G	SPRED1	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 41371	NM_152594.3(SPRED1):c.291G>A (p.Lys97=)	SPRED1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GBenign
Select item 41452	NM_152594.3(SPRED1):c.424-18G>A	SPRED1	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 41453	NM_152594.3(SPRED1):c.424-8C>A	SPRED1	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 468798	NM_152594.3(SPRED1):c.446G>A (p.Ser149Asn)	SPRED1 (S149N)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 47969	NM_152594.3(SPRED1):c.583-7A>G	SPRED1	Single nucleotide variant (intron variant)	Noonan syndrome and Noonan-related syndrome +3 more	GBenign/Likely benign
Select item 47970	NM_152594.3(SPRED1):c.675C>T (p.Ser225=)	SPRED1	Single nucleotide variant (synonymous variant)	Legius syndrome +4 more	GBenign/Likely benign
Select item 241990	NM_152594.3(SPRED1):c.685-8T>C	SPRED1	Single nucleotide variant (intron variant)	Noonan syndrome and Noonan-related syndrome +3 more	GBenign/Likely benign
Select item 241991	NM_152594.3(SPRED1):c.886T>C (p.Cys296Arg)	SPRED1 (C296R)	Single nucleotide variant (missense variant)	Legius syndrome +1 more	GLikely benign
Select item 41370	NM_152594.3(SPRED1):c.1044T>C (p.Val348=)	SPRED1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GBenign