ClinVar Miner

List of variants in gene KIF1B reported as uncertain significance by Molecular Genetics Laboratory,London Health Sciences Centre

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Total variants: 35
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HGVS dbSNP
NM_001365951.3(KIF1B):c.1427G>T (p.Arg476Leu)
NM_001365951.3(KIF1B):c.1629G>T (p.Met543Ile)
NM_001365951.3(KIF1B):c.1769G>A (p.Ser590Asn)
NM_001365951.3(KIF1B):c.183A>G (p.Ser61=)
NM_001365951.3(KIF1B):c.1945_1947del (p.Ser649del)
NM_001365951.3(KIF1B):c.1958C>A (p.Pro653His)
NM_001365951.3(KIF1B):c.2846C>T (p.Thr949Met)
NM_001365951.3(KIF1B):c.3229C>T (p.Pro1077Ser)
NM_001365951.3(KIF1B):c.3259+3A>C
NM_001365951.3(KIF1B):c.4256G>A (p.Arg1419His)
NM_001365951.3(KIF1B):c.4298C>T (p.Pro1433Leu)
NM_001365951.3(KIF1B):c.4409C>T (p.Ala1470Val)
NM_001365951.3(KIF1B):c.4810G>A (p.Val1604Ile)
NM_001365951.3(KIF1B):c.4844T>C (p.Ile1615Thr)
NM_001365951.3(KIF1B):c.4966C>T (p.Arg1656Trp)
NM_001365951.3(KIF1B):c.5231T>C (p.Ile1744Thr)
NM_001365951.3(KIF1B):c.5332C>G (p.Leu1778Val)
NM_001365951.3(KIF1B):c.65A>G (p.Lys22Arg) rs762280202
NM_001365951.3(KIF1B):c.710C>T (p.Ser237Phe)
NM_001365951.3(KIF1B):c.959-16T>A
NM_015074.3(KIF1B):c.1456C>G (p.Pro486Ala) rs201500946
NM_015074.3(KIF1B):c.146C>A (p.Ser49Tyr) rs143654307
NM_015074.3(KIF1B):c.1633G>A (p.Gly545Arg) rs145266399
NM_015074.3(KIF1B):c.1817C>T (p.Thr606Ile) rs142881321
NM_015074.3(KIF1B):c.2021C>T (p.Thr674Ile) rs41274468
NM_015074.3(KIF1B):c.2413T>A (p.Leu805Met) rs139572764
NM_015074.3(KIF1B):c.2480C>T (p.Thr827Ile) rs121908162
NM_015074.3(KIF1B):c.2689G>A (p.Ala897Thr) rs142567076
NM_015074.3(KIF1B):c.2905G>A (p.Ala969Thr) rs200614254
NM_015074.3(KIF1B):c.3002C>T (p.Ser1001Leu)
NM_015074.3(KIF1B):c.3269T>C (p.Ile1090Thr) rs374098797
NM_015074.3(KIF1B):c.3686C>G (p.Thr1229Arg) rs749610931
NM_015074.3(KIF1B):c.3754A>G (p.Ile1252Val) rs529804940
NM_015074.3(KIF1B):c.4073T>C (p.Val1358Ala) rs200561798
NM_015074.3(KIF1B):c.881A>G (p.Lys294Arg) rs373698346

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