List of variants in gene KIF11 reported as uncertain significance for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_004523.4(KIF11):c.1495-3T>C	rs192601648	0.00006
NM_004523.4(KIF11):c.574-5G>T	rs781705800	0.00004
NM_004523.4(KIF11):c.1681G>A (p.Glu561Lys)	rs758761887	0.00002
NM_004523.4(KIF11):c.2831G>A (p.Arg944His)	rs756134992	0.00001
NM_004523.4(KIF11):c.979C>T (p.Arg327Cys)	rs191708835	0.00001
NM_004523.4(KIF11):c.1256T>A (p.Ile419Asn)
NM_004523.4(KIF11):c.1333A>T (p.Asn445Tyr)
NM_004523.4(KIF11):c.164G>C (p.Gly55Ala)
NM_004523.4(KIF11):c.2273C>A (p.Ser758Tyr)
NM_004523.4(KIF11):c.2341C>G (p.Gln781Glu)
NM_004523.4(KIF11):c.2633A>G (p.Asn878Ser)
NM_004523.4(KIF11):c.2830C>T (p.Arg944Cys)	rs387906642
NM_004523.4(KIF11):c.3166C>A (p.Leu1056Ile)	rs1845014504
NM_004523.4(KIF11):c.539A>G (p.Glu180Gly)

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