SFMBT1[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2653900	NM_016329.4(SFMBT1):c.1440C>T (p.His480=)	SFMBT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 770532	NM_016329.4(SFMBT1):c.1360C>T (p.Arg454Cys)	SFMBT1 (R454C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 769604	NM_016329.4(SFMBT1):c.999C>T (p.Phe333=)	SFMBT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775878	NM_016329.4(SFMBT1):c.941G>T (p.Arg314Leu)	SFMBT1 (R314L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 770533	NM_016329.4(SFMBT1):c.819T>C (p.His273=)	SFMBT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 785053	NM_016329.4(SFMBT1):c.462T>C (p.Asn154=)	SFMBT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 156849	NM_016329.4(SFMBT1):c.-130-31769_-130-30020del	SFMBT1	Deletion (intron variant)	Large for gestational age +2 more	Gnot provided

ClinVar