"Clinical Genetics, Academic Medical Center"[submitter] AND "KIF11"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 726756	NM_004523.4(KIF11):c.77+5G>C	KIF11	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 1168099	NM_004523.4(KIF11):c.77+9_77+11del	KIF11	Deletion (intron variant)	KIF11-related disorder +1 more	GBenign/Likely benign
Select item 771176	NM_004523.4(KIF11):c.1706A>G (p.Asn569Ser)	KIF11 (N569S)	Single nucleotide variant (missense variant)	KIF11-related disorder +1 more	GLikely benign
Select item 259409	NM_004523.4(KIF11):c.2153A>T (p.His718Leu)	KIF11 (H718L)	Single nucleotide variant (missense variant)	Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability +2 more	GBenign
Select item 738646	NM_004523.4(KIF11):c.2166T>G (p.Leu722=)	KIF11	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 259410	NM_004523.4(KIF11):c.2770+16A>G	KIF11	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 714223	NM_004523.4(KIF11):c.2775G>A (p.Thr925=)	KIF11	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 235554	NM_004523.4(KIF11):c.3126G>C (p.Leu1042Phe)	KIF11 (L1042F)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign

ClinVar