ClinVar Miner

List of variants in gene KIF1B reported as likely benign for not provided

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Total variants: 32
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HGVS dbSNP
NM_001365951.3(KIF1B):c.1162C>T (p.Leu388=) rs1569678310
NM_001365951.3(KIF1B):c.1623A>G (p.Pro541=) rs753016667
NM_001365951.3(KIF1B):c.1861+9G>A rs1283855085
NM_001365951.3(KIF1B):c.213C>T (p.Asn71=) rs765503412
NM_001365951.3(KIF1B):c.2727C>T (p.Pro909=) rs200858074
NM_001365951.3(KIF1B):c.2829C>T (p.Ala943=) rs745644299
NM_001365951.3(KIF1B):c.2934T>G (p.Val978=) rs749154726
NM_001365951.3(KIF1B):c.3393A>C (p.Pro1131=) rs1569854004
NM_001365951.3(KIF1B):c.3909G>C (p.Gly1303=) rs1569872691
NM_001365951.3(KIF1B):c.3949+9G>A rs758193519
NM_001365951.3(KIF1B):c.4356A>G (p.Thr1452=) rs150358670
NM_001365951.3(KIF1B):c.4524C>T (p.Thr1508=) rs373636782
NM_001365951.3(KIF1B):c.5442G>A (p.Ser1814=) rs188387287
NM_001365951.3(KIF1B):c.60C>G (p.Thr20=) rs751386973
NM_001365951.3(KIF1B):c.753A>C (p.Gly251=) rs537439756
NM_015074.3(KIF1B):c.1401A>T (p.Gly467=) rs757451919
NM_015074.3(KIF1B):c.1419T>C (p.Asp473=) rs146364486
NM_015074.3(KIF1B):c.1640-5C>T rs567968956
NM_015074.3(KIF1B):c.1644C>T (p.Ile548=) rs774839409
NM_015074.3(KIF1B):c.1977+6360G>T rs41274458
NM_015074.3(KIF1B):c.1977+6625G>A rs145248590
NM_015074.3(KIF1B):c.1977+6956A>G rs148481786
NM_015074.3(KIF1B):c.2172C>T (p.Ala724=) rs749823391
NM_015074.3(KIF1B):c.2328C>T (p.Arg776=) rs753982918
NM_015074.3(KIF1B):c.2413T>A (p.Leu805Met) rs139572764
NM_015074.3(KIF1B):c.2466C>T (p.Asp822=) rs145846362
NM_015074.3(KIF1B):c.3107G>A (p.Arg1036Gln) rs745363423
NM_015074.3(KIF1B):c.364-10A>G rs886044966
NM_015074.3(KIF1B):c.5294C>T (p.Pro1765Leu) rs61999305
NM_015074.3(KIF1B):c.608+8dup rs139613776
NM_015074.3(KIF1B):c.85C>G (p.Gln29Glu) rs760368705
NM_015074.3(KIF1B):c.924C>T (p.Leu308=) rs1060504381

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