ClinVar Miner

List of variants in gene KIF5C reported as uncertain significance for not provided

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Total variants: 38
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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.2675G>A (p.Arg892Gln) rs777411017 0.00013
NM_004522.3(KIF5C):c.1405G>A (p.Glu469Lys) rs753378799 0.00002
NM_004522.3(KIF5C):c.116T>C (p.Val39Ala) rs1190316056 0.00001
NM_004522.3(KIF5C):c.2073G>A (p.Thr691=) rs181099929 0.00001
NM_004522.3(KIF5C):c.2497A>G (p.Lys833Glu) rs774772941 0.00001
NM_004522.3(KIF5C):c.2779C>T (p.Arg927Cys) rs867604993 0.00001
NM_004522.3(KIF5C):c.292-2225G>C rs1558904703 0.00001
NM_004522.3(KIF5C):c.1187C>A (p.Thr396Asn) rs761630242
NM_004522.3(KIF5C):c.1355A>C (p.Gln452Pro)
NM_004522.3(KIF5C):c.1600A>G (p.Ser534Gly)
NM_004522.3(KIF5C):c.1850G>A (p.Arg617Lys)
NM_004522.3(KIF5C):c.1984G>C (p.Asp662His) rs1681611679
NM_004522.3(KIF5C):c.1_3del (p.Met1del) rs2468129311
NM_004522.3(KIF5C):c.2100+1G>T rs2468300960
NM_004522.3(KIF5C):c.2215A>C (p.Asn739His)
NM_004522.3(KIF5C):c.2230del (p.Leu744fs)
NM_004522.3(KIF5C):c.2263A>G (p.Lys755Glu) rs1292026609
NM_004522.3(KIF5C):c.2354A>G (p.Lys785Arg)
NM_004522.3(KIF5C):c.2446-5T>A rs2468318668
NM_004522.3(KIF5C):c.254A>G (p.Tyr85Cys)
NM_004522.3(KIF5C):c.2558G>A (p.Arg853Gln)
NM_004522.3(KIF5C):c.2687G>A (p.Arg896His) rs756942747
NM_004522.3(KIF5C):c.2731A>G (p.Lys911Glu) rs1682149018
NM_004522.3(KIF5C):c.2773C>G (p.Pro925Ala)
NM_004522.3(KIF5C):c.289G>A (p.Glu97Lys)
NM_004522.3(KIF5C):c.362A>G (p.Tyr121Cys) rs1682312340
NM_004522.3(KIF5C):c.37T>C (p.Cys13Arg) rs754239937
NM_004522.3(KIF5C):c.397-1G>A
NM_004522.3(KIF5C):c.397G>T (p.Val133Phe)
NM_004522.3(KIF5C):c.487G>C (p.Val163Leu) rs1574771539
NM_004522.3(KIF5C):c.676G>T (p.Gly226Trp)
NM_004522.3(KIF5C):c.76G>A (p.Gly26Arg)
NM_004522.3(KIF5C):c.793G>A (p.Val265Met)
NM_004522.3(KIF5C):c.838C>T (p.Arg280Trp)
NM_004522.3(KIF5C):c.865C>T (p.Gln289Ter)
NM_004522.3(KIF5C):c.949A>G (p.Thr317Ala)

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