List of variants in gene KIF11 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_004523.4(KIF11):c.193A>G (p.Thr65Ala)	rs200410468	0.00009
NM_004523.4(KIF11):c.455C>T (p.Thr152Ile)	rs140534766	0.00004
NM_004523.4(KIF11):c.1075A>G (p.Ile359Val)	rs1457816296	0.00001
NM_004523.4(KIF11):c.1677G>A (p.Met559Ile)	rs750869480	0.00001
NM_004523.4(KIF11):c.1305G>A (p.Arg435=)	rs1554861552
NM_004523.4(KIF11):c.179A>T (p.Lys60Met)	rs1298166671
NM_004523.4(KIF11):c.2461T>C (p.Ser821Pro)	rs2135923469
NM_004523.4(KIF11):c.2922G>A (p.Pro974=)

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