List of variants in gene KIF5C reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004522.3(KIF5C):c.576C>T (p.His192=)	rs376592911	0.00036
NM_004522.3(KIF5C):c.2640G>A (p.Glu880=)	rs376124388	0.00027
NM_004522.3(KIF5C):c.2073G>A (p.Thr691=)	rs181099929	0.00001
NM_004522.3(KIF5C):c.1984G>C (p.Asp662His)	rs1681611679
NM_004522.3(KIF5C):c.2263A>G (p.Lys755Glu)
NM_004522.3(KIF5C):c.2675G>A (p.Arg892Gln)
NM_004522.3(KIF5C):c.2687G>A (p.Arg896His)
NM_004522.3(KIF5C):c.2731A>G (p.Lys911Glu)	rs1682149018
NM_004522.3(KIF5C):c.2779C>T (p.Arg927Cys)	rs867604993
NM_004522.3(KIF5C):c.37T>C (p.Cys13Arg)

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