"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "KIFBP"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 158698	NM_015634.4(KIFBP):c.68A>G (p.Glu23Gly)	LOC130003959, KIFBP (E23G)	Single nucleotide variant (missense variant)	KIFBP-related condition +3 more	GBenign/Likely benign
Select item 158697	NM_015634.4(KIFBP):c.518T>C (p.Met173Thr)	KIFBP (M173T)	Single nucleotide variant (missense variant)	KIFBP-related condition +3 more	GBenign/Likely benign
Select item 2640541	NM_015634.4(KIFBP):c.819A>G (p.Leu273=)	KIFBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2640542	NM_015634.4(KIFBP):c.1101C>T (p.Thr367=)	KIFBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1675421	NM_015634.4(KIFBP):c.1110G>A (p.Leu370=)	KIFBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 623737	NM_015634.4(KIFBP):c.1252G>A (p.Asp418Asn)	KIFBP (D418N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 211258	NM_015634.4(KIFBP):c.1326A>G (p.Arg442=)	KIFBP	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 158695	NM_015634.4(KIFBP):c.1761T>C (p.Pro587=)	KIFBP	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign

ClinVar